Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- V. Mueller COOLEY AORTA RETRACTOR BLADE LENGTH 4.4 & 2.2CM BLADE 1/2" (1.3CM) WIDE OVERALL LENGTH 8" (20.3CM) FDA UDI
- Model / Reference
- CH8131 FDA UDI
- Description
- V. Mueller COOLEY AORTA RETRACTOR BLADE LENGTH 4.4 & 2.2CM BLADE 1/2" (1.3CM) WIDE OVERALL LENGTH 8" (20.3CM) FDA UDI
Identifiers
- Catalog Number
- CH8131 FDA UDI
- Primary DI / UDI-DI
- 10885403034466 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Hand-held surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 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
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
V. Mueller by Carefusion 2200, Inc. — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI dce9c09b-f097-4608-8caa-835ccbb6a5f5 36 fields · synced Sep 18, 2026