Identity
- Trade Name
- STAGEONE SELECT FDA UDI
- Generic Name
- Orthopaedic cement spacer mould FDA UDI
- Model / Reference
- 431199 FDA UDI
Identifiers
- Catalog Number
- 431199 FDA UDI
- Primary DI / UDI-DI
- 00880304521162 FDA UDI
- FDA Product Code
- KWY FDA UDIKWL FDA UDIMBB FDA UDI
- GMDN Term
- Orthopaedic cement spacer mould FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3390 FDA UDI888.3360 FDA UDI888.3027 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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: Orthopaedic cement spacer mould
Stageone Select by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic cement spacer mould.
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Cleared under the same submission
K080979 also covers:
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
K161166 also covers:
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
K222760 also covers:
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
- StageOne Select — Biomet Orthopedics, Inc.
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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 0212636f-dbd4-46d5-8ba1-aef70f82caba 36 fields · synced Jun 8, 2026