Identity
- Trade Name
- Arjo Slides Sheet FDA UDI
- Generic Name
- Patient transfer sliding mat FDA UDI
- Device Name
- Arjo slide tube radiology [MaxiTube Radiology] FDA UDI
- Model / Reference
- NSAV5060 FDA UDI
- Description
- Arjo slide tube radiology [MaxiTube Radiology] FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055982789837 FDA UDI
- FDA Product Code
- IKX FDA UDI
- GMDN Term
- Patient transfer sliding mat FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Patient transfer sliding mat
Arjo Slides Sheet by Arjohuntleigh, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- AirPal Repositioning Sheet — RENU MEDICAL, INC · Class I
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
- Arjohuntleigh, Inc.
Sources (1)
- FDA UDI 53a0674b-e593-4a98-83a6-27cb1f0cea6e 33 fields · synced May 31, 2026