Identity
- Trade Name
- Wagner SL Revision® FDA UDI
- Generic Name
- Revision uncoated hip femur prosthesis FDA UDI
- Model / Reference
- 01.00102.622 FDA UDI
Identifiers
- Catalog Number
- 01.00102.622 FDA UDI
- Primary DI / UDI-DI
- 00889024485372 FDA UDI
- FDA Product Code
- LZO FDA UDI
- GMDN Term
- Revision uncoated hip femur prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3353 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 265 Millimeter FDA UDIOuter Diameter — 22 Millimeter FDA UDI
Category: Revision uncoated hip femur prosthesis
Wagner SL Revision® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Revision uncoated hip femur prosthesis.
- SPII Model Lubinus — WALDEMAR LINK GmbH & Co. KG · Class II
- Alteon — Exactech, Inc. · Class II
- Alteon — Exactech, Inc. · Class II
- Megasystem C — WALDEMAR LINK GmbH & Co. KG · Class II
- Alteon — Exactech, Inc. · Class II
- Revival Modular Hip Stem — CORIN LTD · Class II
- SPII Model Lubinus — WALDEMAR LINK GmbH & Co. KG · Class II
- Alteon — Exactech, Inc. · Class II
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 |
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Manufacturer
- Manufacturer
- Zimmer, Inc.
Sources (1)
- FDA UDI c3baa0e3-74ec-4d28-a100-7ef344f0f803 35 fields · synced May 31, 2026