Identity
- Trade Name
- Slide Sheet EUDAMEDArjo Slides Sheet FDA UDI
- Generic Name
- Patient transfer sliding mat FDA UDI
- Device Name
- Disposable Slide Sheet EUDAMEDArjo slide sheet - XXL [MaxiSlide Sheet XXL] FDA UDIArjo slide sheet [MaxiSlide sheet] FDA UDI
- Model / Reference
- NSA0500 EUDAMEDFDA UDINPA0500 EUDAMEDNSAV5000 FDA UDI
- Description
- Arjo slide sheet - XXL [MaxiSlide Sheet XXL] FDA UDIArjo slide sheet [MaxiSlide sheet] FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055982789653 EUDAMEDFDA UDI05055982789820 FDA UDI
- Basic UDI-DI
- 5060693520204VR EUDAMED
- FDA Product Code
- IKX FDA UDI
- EMDN Code
- V08050399 PATIENT TRANSFER LIFTS - OTHER EUDAMED
- GMDN Term
- Patient transfer sliding mat FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.5050 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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 — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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- AirPal Repositioning Sheet — RENU MEDICAL, INC · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Arjohuntleigh, Inc.
Sources (3)
- FDA UDI a04fec9e-b8dc-4533-bcfd-92412b54c174 33 fields · synced Jul 13, 2026
- FDA UDI 424786f6-9e3a-426e-8a07-6572da334f67 33 fields · synced May 30, 2026
- EUDAMED 107d3478-33a8-426b-b4d3-0ba50433efc4 61 fields · synced Jul 13, 2026