← Back to catalogue

Medi-Glide

FDA UDI

Class I (US FDA UDI)

by Medi Care System Slu

Identity

Trade Name
Medi-Glide FDA UDI
Generic Name
Patient transfer sliding board FDA UDI
Device Name
Rigid board for transfer from bed to stretcher FDA UDI
Model / Reference
TMG6430 FDA UDI
Description
Rigid board for transfer from bed to stretcher FDA UDI

Identifiers

Primary DI / UDI-DI
08436035352395 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer sliding board 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 board

Medi-Glide 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 board.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b3f2aad4-b180-4882-8c56-4d0883bbc5f4 34 fields · synced Jun 1, 2026