Identity
- Trade Name
- Foot and Ankle Stand FDA UDI
- Generic Name
- Diagnostic X-ray system positioning frame FDA UDI
- Model / Reference
- G1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860008892768 FDA UDI
- FDA Product Code
- IYB FDA UDI
- GMDN Term
- Diagnostic X-ray system positioning frame FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1770 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Diagnostic X-ray system positioning frame
Foot and Ankle Stand by Oxos Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Diagnostic X-ray system positioning frame.
- CombiMax — Pausch, L.L.C. · Class II
- CombiMax — Pausch, L.L.C. · Class II
- ElevatorMax — Pausch, L.L.C. · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Oxos Medical
Sources (1)
- FDA UDI 2e7b0b2e-c610-4797-9e12-b6be925a37d5 33 fields · synced May 30, 2026