Identity
- Trade Name
- Optimos™ Snare FDA UDI
- Generic Name
- Mechanical-cutting endoscopic polypectomy snare FDA UDI
- Device Name
- The Optimos™ Snare is designed to be used for without diathermic energy for the endoscopic resection of polyp tissue in the gastrointestinal tract. FDA UDI
- Model / Reference
- KSN22FHC-20 FDA UDI
- Description
- The Optimos™ Snare is designed to be used for without diathermic energy for the endoscopic resection of polyp tissue in the gastrointestinal tract. FDA UDI
Identifiers
- Catalog Number
- KSN22FHC-20 FDA UDI
- Primary DI / UDI-DI
- 08809744976228 FDA UDI
- FDA Product Code
- FGX FDA UDI
- GMDN Term
- Mechanical-cutting endoscopic polypectomy snare FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4730 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Mechanical-cutting endoscopic polypectomy snare
Optimos™ Snare by Taewoong Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mechanical-cutting endoscopic polypectomy snare.
- LesionHunter(TM) Rotatable Nitinol Cold Snare — Micro-Tech (Nanjing) Co., Ltd. · Class I
- Multiple Loop Polypectomy Snare — Avanos Medical, Inc. · Class II
- Disposable Polypectomy Cold Snare — Yangzhou Fartley Medical Instrument Technology Co., Ltd. · Class I
- LesionHunter(TM) Rotatable Nitinol Cold Snare — Micro-Tech (Nanjing) Co., Ltd. · Class I
- Multiple Loop Polypectomy Snare — Avanos Medical, Inc. · Class II
- CAPTIFLEX — Boston Scientific · Class II
- Lasso — Diversatek Healthcare · Class I
- Cold Snare — Micro-Tech (Nanjing) Co., Ltd. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Taewoong Medical
Sources (1)
- FDA UDI 54495042-4ac7-4a5f-a63c-da4814464336 35 fields · synced Jun 1, 2026