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Medline-Microtek

FDA UDI

Class I (US FDA UDI)

by Microtek Medical LLC

Identity

Trade Name
Medline-Microtek FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
KNEE AND BODY STRAP, DISPOSABLE, NONWOVEN, TWO PIECE, 4" X 60" FDA UDI
Model / Reference
Protective Restraints FDA UDI
Description
KNEE AND BODY STRAP, DISPOSABLE, NONWOVEN, TWO PIECE, 4" X 60" FDA UDI

Identifiers

Catalog Number
PSKB100N FDA UDI
Primary DI / UDI-DI
10748426141125 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, single-use

Medline-Microtek by Microtek Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 77cf4491-7f76-4239-bf8f-a3867a7195e2 34 fields · synced Jun 8, 2026