Identity
- Trade Name
- Quickie 5R FDA UDI
- Generic Name
- Push-rim manual wheelchair, non-bariatric FDA UDI
- Device Name
- The Quickie® 5R is designed to deliver superior rigid wheelchair performance day after day. As you and your environment evolve, or as you refine your riding capabilities, the 5R's frame and components adjust to elevate your mobility. FDA UDI
- Model / Reference
- 5R FDA UDI
- Description
- The Quickie® 5R is designed to deliver superior rigid wheelchair performance day after day. As you and your environment evolve, or as you refine your riding capabilities, the 5R's frame and components adjust to elevate your mobility. FDA UDI
Identifiers
- Catalog Number
- EIR10 FDA UDI
- Primary DI / UDI-DI
- 00016958060089 FDA UDI
- FDA Product Code
- IOR FDA UDI
- GMDN Term
- Push-rim manual wheelchair, non-bariatric 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Quickie 5R 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 ec99e989-0b66-47e9-ae47-0f30effabeb7 35 fields · synced Jun 9, 2026