Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Surgical retractor/retraction system blade, reusable FDA UDI
- Device Name
- V. Mueller KENNERDELL-MAROON ORBITAL RETRACTOR BLADES MALLEABLE, COPPER 50 X 8MM WIDE FDA UDI
- Model / Reference
- NL1175-005 FDA UDI
- Description
- V. Mueller KENNERDELL-MAROON ORBITAL RETRACTOR BLADES MALLEABLE, COPPER 50 X 8MM WIDE FDA UDI
Identifiers
- Catalog Number
- NL1175-005 FDA UDI
- Primary DI / UDI-DI
- 10885403070907 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Surgical retractor/retraction system blade, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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 |
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Manufacturer
- Manufacturer
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 52aff5eb-8231-4a8b-bc23-dcd23a299138 36 fields · synced Sep 18, 2026