Identity
- Trade Name
- RHEAD FDA UDI
- Generic Name
- Elbow radius prosthesis FDA UDI
- Device Name
- Radial head implant , Size 2 FDA UDI
- Model / Reference
- RHA-H2 FDA UDI
- Description
- Radial head implant , Size 2 FDA UDI
Identifiers
- Catalog Number
- RHA-H2 FDA UDI
- Primary DI / UDI-DI
- 00886385024660 FDA UDI
- FDA Product Code
- KWI FDA UDI
- GMDN Term
- Elbow radius prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3170 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: Elbow radius prosthesis
Rhead by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Elbow radius prosthesis.
- LATITUDE EV™ — TORNIER, INC. · Class II
- Seitz Solution Radial Head — Kapp Surgical Instrument, Inc. · Class II
- Seitz Solution Radial Head — Kapp Surgical Instrument, Inc. · Class II
- Avenger — In2Bones, USA · Class II
- Align — SKELETAL DYNAMICS L.L.C. · Class II
- Seitz Solution Radial Head — Kapp Surgical Instrument, Inc. · Class II
- LATITUDE EV™ — TORNIER, INC. · Class II
- L2L® — Zimmer, Inc. · 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
- Stryker Corp.
Sources (1)
- FDA UDI f2b991a6-6307-4569-9cbc-fe27c6730450 34 fields · synced Jun 1, 2026