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Sign in to claim this brandKossel Medtech (Suzhou) Co., Ltd.
US
Last updated May 23, 2026
What Kossel Medtech (Suzhou) Co., Ltd. makes
The company manufactures coronary angioplasty balloon catheters designed for percutaneous transluminal coronary angioplasty (PTCA), including non-compliant (NC) and standard variants. These devices are intended for dilating narrowed coronary arteries to restore blood flow, with some models incorporating perfusion capabilities to maintain blood supply during the procedure.
The portfolio includes devices classified as Class II and Class III under regulatory frameworks, with authorisations granted through FDA 510(k) submissions and FDA Unique Device Identification (UDI) listings. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 560219894
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Kossel Medtech (suzhou) Co., Ltd. Suzhou Jiangsu · CN FEI 3014390222