Identity
- Trade Name
- Small Prone Stander FDA UDI
- Generic Name
- Manual stander FDA UDI
- Device Name
- Prone Stander FDA UDI
- Model / Reference
- E930 FDA UDI
- Description
- Prone Stander FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858101008094 FDA UDI
- FDA Product Code
- KNL FDA UDI
- GMDN Term
- Manual stander FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5370 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Small Prone Stander by Rifton Equipment — 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
- Rifton Equipment
Sources (1)
- FDA UDI bd894806-2f0c-47b9-96ee-f5d80286b92e 35 fields · synced May 30, 2026