Identity
- Trade Name
- KMEDIC FDA UDI
- Generic Name
- Wire holding/twisting forceps FDA UDI
- Device Name
- WIRE PULLING FORCEPS 6 1/2" FDA UDI
- Model / Reference
- IPN013939 FDA UDI
- Description
- WIRE PULLING FORCEPS 6 1/2" FDA UDI
Identifiers
- Catalog Number
- KM46637 FDA UDI
- Primary DI / UDI-DI
- 24026704271898 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Wire holding/twisting forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 16.5 Centimeter FDA UDI
Category: Wire holding/twisting forceps
Kmedic by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wire holding/twisting forceps.
- WAVY FRENCH BENDER — ETABLISSEMENTS OURY GUYE ET FILS · Class I
- CANULA TAP 4.5 FOR SCREW 6.5 — groupe lépine · Class I
- ROCCIA MultiLIF, ALIF, TLIF — SILONY MEDICAL GMBH · Class I
- Raszpla — ChM spółka z ograniczoną odpowiedzialnością · Class I
- Preparator — ChM spółka z ograniczoną odpowiedzialnością · Class I
- Retraktor — ChM spółka z ograniczoną odpowiedzialnością · Class I
- Trokar — ChM spółka z ograniczoną odpowiedzialnością · Class I
- SYMPHONY OCT SYSTEM — MEDOS INTERNATIONAL SARL · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 56a08ba6-0646-48ed-8c2c-bbda84dfa3b3 36 fields · synced Jun 6, 2026