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   <title>Peijia Medical submits EU regulatory application for heart device</title>
   <link>http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</link>
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&lt;p&gt;Peijia Medical Limited (HKEX: 9996) submitted a European Union Medical Device Regulation CE Mark registration application for its GeminiOne Transcatheter Edge-to-Edge Repair system, the Hong Kong-based company announced. The device treats mitral regurgitation through a minimally invasive cardiac procedure.&lt;/p&gt;

&lt;p&gt;The GeminiOne system features a sliding groove mechanism designed to enable longer coaptation length while maintaining a smaller implant size. The device includes an independent leaflet grasping design, an auto-locking mechanism, and multi-angular detachment capability to accommodate various anatomical variations.&lt;/p&gt;

&lt;p&gt;HighLife SAS serves as the company's European partner for the regulatory submission process. The system has received patents globally and has undergone multiple</description>
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   <pubDate>Mon, 09 Feb 2026 01:00:15 -0500</pubDate>
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   <title>Peijia Medical submits EU regulatory application for heart device</title>
   <link>http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</link>
   <description>

&lt;p&gt;Peijia Medical Limited (HKEX: 9996) submitted a European Union Medical Device Regulation CE Mark registration application for its GeminiOne Transcatheter Edge-to-Edge Repair system, the Hong Kong-based company announced. The device treats mitral regurgitation through a minimally invasive cardiac procedure.&lt;/p&gt;

&lt;p&gt;The GeminiOne system features a sliding groove mechanism designed to enable longer coaptation length while maintaining a smaller implant size. The device includes an independent leaflet grasping design, an auto-locking mechanism, and multi-angular detachment capability to accommodate various anatomical variations.&lt;/p&gt;

&lt;p&gt;HighLife SAS serves as the company's European partner for the regulatory submission process. The system has received patents globally and has undergone multiple</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</guid>
   <pubDate>Mon, 09 Feb 2026 01:00:15 -0500</pubDate>
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   <title>Peijia Medical submits EU regulatory application for heart device</title>
   <link>http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</link>
   <description>

&lt;p&gt;Peijia Medical Limited (HKEX: 9996) submitted a European Union Medical Device Regulation CE Mark registration application for its GeminiOne Transcatheter Edge-to-Edge Repair system, the Hong Kong-based company announced. The device treats mitral regurgitation through a minimally invasive cardiac procedure.&lt;/p&gt;

&lt;p&gt;The GeminiOne system features a sliding groove mechanism designed to enable longer coaptation length while maintaining a smaller implant size. The device includes an independent leaflet grasping design, an auto-locking mechanism, and multi-angular detachment capability to accommodate various anatomical variations.&lt;/p&gt;

&lt;p&gt;HighLife SAS serves as the company's European partner for the regulatory submission process. The system has received patents globally and has undergone multiple</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</guid>
   <pubDate>Mon, 09 Feb 2026 01:00:15 -0500</pubDate>
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   <title>Peijia Medical submits EU regulatory application for heart device</title>
   <link>http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</link>
   <description>

&lt;p&gt;Peijia Medical Limited (HKEX: 9996) submitted a European Union Medical Device Regulation CE Mark registration application for its GeminiOne Transcatheter Edge-to-Edge Repair system, the Hong Kong-based company announced. The device treats mitral regurgitation through a minimally invasive cardiac procedure.&lt;/p&gt;

&lt;p&gt;The GeminiOne system features a sliding groove mechanism designed to enable longer coaptation length while maintaining a smaller implant size. The device includes an independent leaflet grasping design, an auto-locking mechanism, and multi-angular detachment capability to accommodate various anatomical variations.&lt;/p&gt;

&lt;p&gt;HighLife SAS serves as the company's European partner for the regulatory submission process. The system has received patents globally and has undergone multiple</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Peijia+Medical+submits+EU+regulatory+application+for+heart+device/25963648.html</guid>
   <pubDate>Mon, 09 Feb 2026 01:00:15 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/Press+Releases/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/Press+Releases/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/Press+Releases/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/Press+Releases/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/PRNewswire/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/PRNewswire/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/PRNewswire/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Submits EU MDR CE Mark Registration Application for GeminiOne® TEER System</title>
   <link>http://www.streetinsider.com/PRNewswire/Peijia+Medical+Submits+EU+MDR+CE+Mark+Registration+Application+for+GeminiOne%C2%AE+TEER+System/25963645.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Feb. 9, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical Limited&lt;/span&gt; (HKEX: 9996) today announced that it has formally submitted the European Union Medical Device Regulation (EU MDR) CE Mark registration application for its internally developed &lt;b&gt;GeminiOne Transcatheter Edge-to-Edge Repair (TEER) System&lt;/b&gt; for the treatment of mitral regurgitation, with HighLife SAS being the Company's European partner.&lt;/p&gt;
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   <pubDate>Mon, 09 Feb 2026 01:00:00 -0500</pubDate>
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   <title>Peijia Medical Receives NMPA Approval for TaurusTrio Transcatheter Aortic Valve System, Pioneering Treatment for Aortic Regurgitation in China</title>
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   <title>Peijia Medical Receives NMPA Approval for TaurusTrio Transcatheter Aortic Valve System, Pioneering Treatment for Aortic Regurgitation in China</title>
   <link>http://www.streetinsider.com/PRNewswire/Peijia+Medical+Receives+NMPA+Approval+for+TaurusTrio+Transcatheter+Aortic+Valve+System%2C+Pioneering+Treatment+for+Aortic+Regurgitation+in+China/25732281.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Dec. 12, 2025&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Peijia Medical (9996.HK), a leading Chinese domestic company in the high-growth transcatheter valve therapeutics and neurovascular interventions markets, announced that its TaurusTrio Transcatheter Aortic Valve (TAV) system received approval from the &lt;span&gt;National Medical Products Administration&lt;/span&gt; (NMPA) of &lt;location value=&quot;LC/cn&quot; idsrc=&quot;xmltag.org&quot; &gt;China&lt;/location&gt; on &lt;chron&gt;December 11, 2025&lt;/chron&gt;.&lt;/p&gt;
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   <pubDate>Fri, 12 Dec 2025 07:30:00 -0500</pubDate>
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   <title>Peijia Medical Announces 2025 Interim Results</title>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LC/hk&quot; idsrc=&quot;xmltag.org&quot; &gt;HONG KONG&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 25, 2025&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;HongKong:9996&quot; idsrc=&quot;xmltag.org&quot; &gt;Peijia Medical&lt;/span&gt; (9996.HK), a leading Chinese domestic player in the high-growth transcatheter valve therapeutics and neurovascular interventions markets, announced financial results for the six months ended &lt;chron&gt;June 30, 2025&lt;/chron&gt; (&quot;the Reporting Period&quot;) on &lt;chron&gt;August 22, 2025&lt;/chron&gt;.&lt;/p&gt;

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   <pubDate>Mon, 25 Aug 2025 08:00:00 -0500</pubDate>
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