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Arjo Slides Sheet

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref NSA0500Model NPA0500

by Arjohuntleigh, Inc.

Identity

Trade Name
Slide Sheet EUDAMED
Arjo Slides Sheet FDA UDI
Generic Name
Patient transfer sliding mat FDA UDI
Device Name
Disposable Slide Sheet EUDAMED
Arjo slide sheet - XXL [MaxiSlide Sheet XXL] FDA UDI
Arjo slide sheet [MaxiSlide sheet] FDA UDI
Model / Reference
NSA0500 EUDAMEDFDA UDI
NPA0500 EUDAMED
NSAV5000 FDA UDI
Description
Arjo slide sheet - XXL [MaxiSlide Sheet XXL] FDA UDI
Arjo slide sheet [MaxiSlide sheet] FDA UDI

Identifiers

Primary DI / UDI-DI
05055982789653 EUDAMEDFDA UDI
05055982789820 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

Similar devices

Also classified as Patient transfer sliding mat.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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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