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Medi-Slide

FDA UDI

Class I (US FDA UDI)

by Medi Care System Slu

Identity

Trade Name
Medi-Slide FDA UDI
Generic Name
Patient transfer sliding mat FDA UDI
Device Name
Padded sliding tubular to reposition patients in bed FDA UDI
Model / Reference
TMS6340 FDA UDI
Description
Padded sliding tubular to reposition patients in bed FDA UDI

Identifiers

Primary DI / UDI-DI
08436035352586 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer sliding mat 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 sliding mat

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

Similar devices

Also classified as Patient transfer sliding mat.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7a1fd0a9-d2f0-4b7f-8911-645e0aa5cdb4 34 fields · synced May 30, 2026