Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Surgical retractor/retraction system blade, reusable FDA UDI
- Device Name
- MCCULLOCH NARROW MUSCLE BLADE SET, INCLUDES 1 PAIR NL9702-121, NL9702-122 NL9702-123, NL9702-124 FDA UDI
- Model / Reference
- NL9702-120 FDA UDI
- Description
- MCCULLOCH NARROW MUSCLE BLADE SET, INCLUDES 1 PAIR NL9702-121, NL9702-122 NL9702-123, NL9702-124 FDA UDI
Identifiers
- Catalog Number
- NL9702-120 FDA UDI
- Primary DI / UDI-DI
- 10885403185106 FDA UDI
- FDA Product Code
- GZT FDA UDI
- GMDN Term
- Surgical retractor/retraction system blade, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4800 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 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 84c16a88-a1b9-429d-9ec0-e17191c21683 36 fields · synced Jun 6, 2026