Identity
- Trade Name
- Hugo FDA UDI
- Generic Name
- Walking aid handgrip FDA UDI
- Device Name
- Canes & CrutchesCrutches Product Description: HUGO AL. CRUTCH TALL, 1PR, 8PR/CV, Ret FDA UDI
- Model / Reference
- 721-780 FDA UDI
- Description
- Canes & CrutchesCrutches Product Description: HUGO AL. CRUTCH TALL, 1PR, 8PR/CV, Ret FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00754021210909 FDA UDI
- FDA Product Code
- IPR FDA UDI
- GMDN Term
- Walking aid handgrip FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3150 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
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
No
FDA UDI
Hugo by Drive Devilbiss Healthcare — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI e86c0f86-586a-438d-9a97-24b0b97e4475 34 fields · synced Jun 8, 2026