Identity
- Trade Name
- MOBILITY ASSIST FDA UDI
- Generic Name
- Gait rehabilitation electronic walker FDA UDI
- Device Name
- Mobility Assist FDA UDI
- Model / Reference
- 950-570 FDA UDI
- Description
- Mobility Assist FDA UDI
Identifiers
- Catalog Number
- 950-570 FDA UDI
- Primary DI / UDI-DI
- 00718175005705 FDA UDI
- FDA Product Code
- BXB FDA UDI
- GMDN Term
- Gait rehabilitation electronic walker FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5380 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
No
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
Category: Gait rehabilitation electronic walker
Mobility Assist by Biodex Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Gait rehabilitation electronic walker.
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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 |
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Manufacturer
- Manufacturer
- Biodex Medical Systems
Sources (1)
- FDA UDI acbae2aa-b92a-423f-8828-1fa3c3175e18 34 fields · synced May 30, 2026