Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Surgical retraction system, reusable FDA UDI
- Device Name
- V. Mueller Neuro/Spine SHADOW-LINE OFFSET LUMBAR RETRACTOR SYSTEM WITH STORAGE CASE FDA UDI
- Model / Reference
- Z-0162 FDA UDI
- Description
- V. Mueller Neuro/Spine SHADOW-LINE OFFSET LUMBAR RETRACTOR SYSTEM WITH STORAGE CASE FDA UDI
Identifiers
- Catalog Number
- Z-0162 FDA UDI
- Primary DI / UDI-DI
- 10885403140815 FDA UDI
- FDA Product Code
- OJG FDA UDI
- GMDN Term
- Surgical retraction system, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 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 af1dcd4f-f411-4e29-9131-de2773b164f5 36 fields · synced Sep 18, 2026