Identity
- Trade Name
- GMRS FDA UDI
- Generic Name
- Press-fit femoral stem prosthesis FDA UDI
- Device Name
- Long Bowed Press-Fit Stem FDA UDI
- Model / Reference
- 6495-5-114 FDA UDI
- Description
- Long Bowed Press-Fit Stem FDA UDI
Identifiers
- Catalog Number
- 6495-5-114 FDA UDI
- Primary DI / UDI-DI
- 07613327033588 FDA UDI
- FDA Product Code
- JDI FDA UDILZO FDA UDIKRO FDA UDI
- GMDN Term
- Press-fit femoral stem prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3350 FDA UDI888.3353 FDA UDI888.3510 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 200.0 Millimeter FDA UDI
Category: Press-fit femoral stem prosthesis
Gmrs by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Press-fit femoral stem prosthesis.
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Cleared under the same submission
K022403 also covers:
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
K023087 also covers:
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
K222056 also covers:
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
- GMRS — Howmedica Osteonics Corp.
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
- Howmedica Osteonics Corp.
Sources (1)
- FDA UDI af72b20b-b981-4b80-95d9-886f58ea9765 36 fields · synced Jun 1, 2026