Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- V. Mueller GENERAL PURPOSE CLAMP SINGLE, CURVED, PAIR FOR VESSELS FROM 0.6 TO 1.4MM FDA UDI
- Model / Reference
- CH13030 FDA UDI
- Description
- V. Mueller GENERAL PURPOSE CLAMP SINGLE, CURVED, PAIR FOR VESSELS FROM 0.6 TO 1.4MM FDA UDI
Identifiers
- Catalog Number
- CH13030 FDA UDI
- Primary DI / UDI-DI
- 70885403124039 FDA UDI
- FDA Product Code
- DXC FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4450 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
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
No
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
V. Mueller by Carefusion 2200, Inc — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Carefusion 2200, Inc
Sources (1)
- FDA UDI 3792e9bb-f91a-46b6-bfac-eb1dcbca7e1f 36 fields · synced Jun 8, 2026