Identity
- Trade Name
- Quickie® Series Manual Wheelchair FDA UDI
- Generic Name
- Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI
- Device Name
- Quickie IRIS Manual Wheelchair FDA UDI
- Model / Reference
- ElZ4-2 FDA UDI
- Description
- Quickie IRIS Manual Wheelchair FDA UDI
Identifiers
- Catalog Number
- ElZ4-2 FDA UDI
- Primary DI / UDI-DI
- 05022408048953 FDA UDI
- FDA Product Code
- IOR FDA UDI
- GMDN Term
- Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3850 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Quickie® Series Manual Wheelchair by Sunrise Medical (US) LLC — 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
- Sunrise Medical (US) LLC
Sources (1)
- FDA UDI 6fe47976-b25d-4756-ba0e-638fe9b29003 36 fields · synced Jun 9, 2026