Identity
- Trade Name
- MRI Stretcher Fowler Back FDA UDI
- Generic Name
- MRI system table, non-powered FDA UDI
- Device Name
- Stretcher, Fowler Back, MRI FDA UDI
- Model / Reference
- 240-110 FDA UDI
- Description
- Stretcher, Fowler Back, MRI FDA UDI
Identifiers
- Catalog Number
- 240-110 FDA UDI
- Primary DI / UDI-DI
- 00718175001103 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- MRI system table, non-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6910 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
Yes
FDA UDI
MR Conditional FDA UDI
MRI Stretcher Fowler Back by Biodex Medical Systems — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Biodex Medical Systems
Sources (1)
- FDA UDI 9abc8240-24c1-4d2b-8446-308548ff55e6 35 fields · synced May 30, 2026