Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- V. Mueller DEBAKEY TITANIUM TISSUE FCPS TIPS 3MM WIDE OVERALL LENGTH 6 inches 15.2CM FDA UDI
- Model / Reference
- CH5912-T FDA UDI
- Description
- V. Mueller DEBAKEY TITANIUM TISSUE FCPS TIPS 3MM WIDE OVERALL LENGTH 6 inches 15.2CM FDA UDI
Identifiers
- Catalog Number
- CH5912T FDA UDI
- Primary DI / UDI-DI
- 10885403029493 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable
V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, reusable.
- Micro-Pliers 17, 5 cm, lightweight, DCL coated — SALVIN DENTAL SPECIALTIES, LLC · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- STILLE Titanium Micro Forceps — Stille AB · Class I
- Gen2 — SURGIX MEDICAL LLC · Class I
- TISSUE FORCEPS SEMKEN 6" SERRATED STRAIGHT — W.H. Holden, Inc. · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Wexler Surgical, Inc. — Wexler Surgical, Inc. · 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
- Steris Corporation
Sources (1)
- FDA UDI 37f0498d-71d8-4a8b-8f88-56e97695a67f 35 fields · synced Jun 8, 2026