SPII Model Lubinus
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- SPII Model Lubinus FDA UDI
- Generic Name
- Revision uncoated hip femur prosthesis FDA UDI
- Device Name
- SPII Model Lubinus Hip Stem EUDAMEDXL Hip Prosthesis Stem,Taper 12/14 FDA UDI
- Model / Reference
- 127-923/35 EUDAMEDFDA UDIHip stem, cemented, CoCrMo, long stem prosthesis, standard neck, 135° CCD EUDAMED
- Description
- XL Hip Prosthesis Stem,Taper 12/14 FDA UDI
Identifiers
- Catalog Number
- 127-923/35 FDA UDI
- Primary DI / UDI-DI
- 04026575025275 EUDAMEDFDA UDI
- Basic UDI-DI
- 4026575-1-HSP-003011-VS EUDAMED
- 510(k) Number
- K953653 FDA UDI
- FDA Product Code
- JDG FDA UDI
- EMDN Code
- P090804030101 REVISION CEMENTED FEMORAL STEMS, WITH FIXED NECK EUDAMED
- GMDN Term
- Revision uncoated hip femur prosthesis FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3360 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
Yes
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
Yes
Manufacturing Date
No
Category: Revision uncoated hip femur prosthesis
SPII Model Lubinus by WALDEMAR LINK GmbH & Co. KG — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Revision uncoated hip femur prosthesis.
- Alteon — Exactech, Inc. · Class II
- Alteon — Exactech, Inc. · Class II
- ZMR® — Zimmer, Inc. · Class II
- Alteon — Exactech, Inc. · Class II
- ZMR® — Zimmer, Inc. · Class II
- Wagner SL Revision® — Zimmer, Inc. · Class II
- ZMR® — Zimmer, Inc. · Class II
- Wagner Cone Prosthesis® — Zimmer, Inc. · Class II
Cleared under the same submission
K953653 also covers:
- Prosthesis Head A — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
- Prosthesis Head B — WALDEMAR LINK GmbH & Co. KG
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- WALDEMAR LINK GmbH & Co. KG
Sources (2)
- FDA UDI 22e4555e-632d-4cb2-8646-41f07c71df25 35 fields · synced Oct 8, 2026
- EUDAMED 6cf8fb8a-1c91-4b08-9920-43fb65d37627 61 fields · synced Oct 8, 2026