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Mobi-tools translide

FDA UDI

Class I (US FDA UDI)

by Medi Care System Slu

Identity

Trade Name
Mobi-tools translide FDA UDI
Generic Name
Patient transfer/turning sheet, single-use FDA UDI
Device Name
Sliding sheet with 8 handles Bariatric 200x90cm to reposition patients FDA UDI
Model / Reference
TTE6142 FDA UDI
Description
Sliding sheet with 8 handles Bariatric 200x90cm to reposition patients FDA UDI

Identifiers

Primary DI / UDI-DI
08436035357864 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer/turning sheet, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Patient transfer/turning sheet, single-use

Mobi-tools translide by Medi Care System Slu — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer/turning sheet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ef2470db-22be-4a8c-8488-251ace7f363e 34 fields · synced May 30, 2026