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Transfer Guide

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Transfer Guide FDA UDI
Generic Name
Patient transfer sliding board FDA UDI
Device Name
Transfer Guide FDA UDI
Model / Reference
MTSBRT014 FDA UDI
Description
Transfer Guide FDA UDI

Identifiers

Catalog Number
MTSBRT014 FDA UDI
Primary DI / UDI-DI
00841439107331 FDA UDI
510(k) Number
K973842 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Patient transfer sliding board FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
Commercial Distribution
Not 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 140 Centimeter FDA UDI
Width — 6.4 Centimeter FDA UDI

Transfer Guide by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K973842 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI 6d4a0625-1c3d-4c01-9623-0455e0523727 38 fields · synced May 30, 2026