Identity
- Trade Name
- S-ROM NOILES FDA UDI
- Generic Name
- Rotating hinged total knee prosthesis FDA UDI
- Device Name
- S-ROM NOILES ROTATING HINGE FEMORAL ROTATING HINGE CEMENTED LEFT X-SMALL FDA UDI
- Model / Reference
- 62-3421L FDA UDI
- Description
- S-ROM NOILES ROTATING HINGE FEMORAL ROTATING HINGE CEMENTED LEFT X-SMALL FDA UDI
Identifiers
- Catalog Number
- 623421L FDA UDI
- Primary DI / UDI-DI
- 10603295179504 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Rotating hinged total knee prosthesis 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
MR Conditional FDA UDI
Category: Rotating hinged total knee prosthesis
S-Rom Noiles by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rotating hinged total knee prosthesis.
- TRIATHLON — Howmedica Osteonics Corp. · Class II
- LEGION — Smith & Nephew, Inc. · Class II
- AS ENDURO — AESCULAP, INC. · Class II
- Endo-Model Standard Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG · Class II
- TRIATHLON — Howmedica Osteonics Corp. · Class II
- Endo-Model Standard Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG · Class II
- LEGION — Smith & Nephew, Inc. · Class II
- Endo-Model Modular Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG · Class II
Cleared under the same submission
K241000 also covers:
- ATTUNE — DEPUY (IRELAND)
- ATTUNE — DEPUY (IRELAND)
- ATTUNE — DEPUY (IRELAND)
- ATTUNE — DEPUY (IRELAND)
- ATTUNE — DEPUY (IRELAND)
- ATTUNE — DEPUY (IRELAND)
- P.F.C. — DEPUY (IRELAND)
- P.F.C. — DEPUY (IRELAND)
- P.F.C. SIGMA — DEPUY (IRELAND)
- P.F.C. SIGMA — DEPUY (IRELAND)
- P.F.C. SIGMA — DEPUY (IRELAND)
- P.F.C. SIGMA — DEPUY (IRELAND)
K905810 also covers:
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
- Depuy (ireland)
Sources (1)
- FDA UDI 30efe484-fbc5-43ac-9290-4a12f1851f7e 36 fields · synced May 31, 2026