Identity
- Trade Name
- Key Surgical Polypectomy Snare FDA UDI
- Generic Name
- Mechanical-cutting endoscopic polypectomy snare FDA UDI
- Device Name
- Polypectomy Snare, Stiff Multi-Wire, Mini-Oval, 10mm W FDA UDI
- Model / Reference
- EN 10330 FDA UDI
- Description
- Polypectomy Snare, Stiff Multi-Wire, Mini-Oval, 10mm W FDA UDI
Identifiers
- Catalog Number
- EN10330 FDA UDI
- Primary DI / UDI-DI
- 00849771039129 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
- Not 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
Key Surgical Polypectomy Snare by Key Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Key Surgical, LLC
Sources (1)
- FDA UDI 5e37c8fa-c7f7-4711-9040-0fac05a49ca0 38 fields · synced May 30, 2026