Identity
- Trade Name
- Rheo Knee FDA UDI
- Generic Name
- Basic power supply, reusable FDA UDI
- Device Name
- KIT POWERSUPPLY PROPRIO/RHEO FDA UDI
- Model / Reference
- PRX00421 FDA UDI
- Description
- KIT POWERSUPPLY PROPRIO/RHEO FDA UDI
Identifiers
- Catalog Number
- PRX00421 FDA UDI
- Primary DI / UDI-DI
- 05690967514341 FDA UDI
- FDA Product Code
- ISW FDA UDI
- GMDN Term
- Basic power supply, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3500 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Rheo Knee by Ossur Americas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Ossur Americas
Sources (1)
- FDA UDI 7da42827-231d-4ca0-9b68-f907b0f97f96 35 fields · synced May 30, 2026