← Back to catalogue
Micro Forceps, Bayonet Round Handle, 1.0mm Ring Tips, 210mm | Kogent
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Micro Forceps, Bayonet Round Handle, 1.0mm Ring Tips, 210mm | Kogent FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Micro Forceps, Bayonet Round Handle, 1.0mm Ring Tips, 210mm | Kogent FDA UDI
- Model / Reference
- N3211-K FDA UDI
- Description
- Micro Forceps, Bayonet Round Handle, 1.0mm Ring Tips, 210mm | Kogent FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840096204360 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Micro Forceps, Bayonet Round Handle, 1.0mm Ring Tips, 210mm | Kogent by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Katalyst Surgical, Llc
Sources (1)
- FDA UDI 0c36547a-e6d0-48dd-a56a-1da89f1645f6 34 fields · synced May 30, 2026