Identity
- Trade Name
- MRI Stretcher FDA UDI
- Generic Name
- MRI system table, non-powered FDA UDI
- Device Name
- This heavy-duty, all aluminum non-magnetic stretcher is ideal for MRI patient transport. FDA UDI
- Model / Reference
- 240-100 FDA UDI
- Description
- This heavy-duty, all aluminum non-magnetic stretcher is ideal for MRI patient transport. FDA UDI
Identifiers
- Catalog Number
- 240-100 FDA UDI
- Primary DI / UDI-DI
- 00879942070750 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
- 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
Category: MRI system table, non-powered
MRI Stretcher by Mirion Technologies (capintec), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as MRI system table, non-powered.
- AADCO — AADCO MEDICAL, INC. · Class II
- MRI Stretcher with Fowler Positioning — MIRION TECHNOLOGIES (CAPINTEC), INC · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mirion Technologies (capintec), Inc
Sources (1)
- FDA UDI 8028860a-08c8-49fd-a2cf-2d290ca74bf9 35 fields · synced Jun 8, 2026