Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Wire-extracting pliers FDA UDI
- Device Name
- Wire Cutting Forceps, 8 3/4", (220 mm), double action, non-sterile, reusable FDA UDI
- Model / Reference
- MG025R FDA UDI
- Description
- Wire Cutting Forceps, 8 3/4", (220 mm), double action, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- MG025R FDA UDI
- Primary DI / UDI-DI
- 04046964573910 FDA UDI
- FDA Product Code
- HXZ FDA UDI
- GMDN Term
- Wire-extracting pliers FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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: Wire-extracting pliers
Aesculap by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wire-extracting pliers.
- gSource — GSOURCE, LLC. · Class I
- Hintermann Series — Vilex, Inc. · Class I
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- SCANLAN® Instrumentation — SCANLAN INTERNATIONAL INC · Class I
- WIRE EXTRACTION PLIERS — SONTEC INSTRUMENTS, INC. · Class I
- PIN PULLER — SONTEC INSTRUMENTS, INC. · Class I
- gSource — GSOURCE, LLC. · Class I
- STEINMANN PIN PULLER — SONTEC INSTRUMENTS, 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
- Aesculap, Inc.
Sources (1)
- FDA UDI 6eefe687-0a95-4583-b6ef-43191e279e02 35 fields · synced May 30, 2026