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Morrison Medical

FDA UDI

Class I (US FDA UDI)

by Morrison Medical, Ltd

Identity

Trade Name
MORRISON MEDICAL FDA UDI
Generic Name
Limb/torso/head restraint, reusable FDA UDI
Device Name
POLY.MTL.PB BKL.ONE PC.7' FDA UDI
Model / Reference
1308BL FDA UDI
Description
POLY.MTL.PB BKL.ONE PC.7' FDA UDI

Identifiers

Catalog Number
1308BL FDA UDI
Primary DI / UDI-DI
00647921130845 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Limb/torso/head restraint, reusable 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Limb/torso/head restraint, reusable

Morrison Medical's POLY.MTL.PB BKL.ONE PC.7' device is a custom-made, non-rigid restraint solution designed for temporary placement on or around the body to restrict movement and facilitate patient positioning during medical procedures. This reusable device features a variety of materials, including nylon, leather, and foam, and is anchored to a fixture or furniture part. It is not intended for immobilization of specific joints.

Similar devices

Also classified as Limb/torso/head restraint, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Morrison Medical, Ltd

Sources (1)

  • FDA UDI c04ecb42-449d-4df6-bf6f-5c052f80c236 35 fields · synced Jul 21, 2026