Identity
- Trade Name
- ACS® FDA UDI
- Generic Name
- Uncoated knee femur prosthesis, metallic FDA UDI
- Device Name
- LD PS femoral component cemented FDA UDI
- Model / Reference
- 42006102 FDA UDI
- Description
- LD PS femoral component cemented FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04048844107642 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Uncoated knee femur prosthesis, metallic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 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
Category: Uncoated knee femur prosthesis, metallic
Acs® by implantcast GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Uncoated knee femur prosthesis, metallic.
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- Orthopedic Salvage System (OSS™) — Biomet Orthopedics, Inc. · Class II
- GMK Sphere Revision System — Medacta International · Class II
- Balance Knee Revision System — ORTHO DEVELOPMENT CORP. · Class II
- LinkSymphoKnee — WALDEMAR LINK GmbH & Co. KG · 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
- implantcast GmbH
Sources (1)
- FDA UDI 9d149690-f3b5-4f1d-8d52-310ff9c0bfe7 34 fields · synced May 30, 2026