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: NYL.PLAS.SR BKL.ONE PC.9' FDA UDI
Model / Reference: 1259MA FDA UDI
Description: NYL.PLAS.SR BKL.ONE PC.9' FDA UDI

Identifiers

Catalog Number: 1259MA FDA UDI
Primary DI / UDI-DI: 00647921125957 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Limb/torso/head restraint, reusable

Morrison Medical by Morrison Medical, Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

E.M Adams co, inc. — E.M. Adams · Class I
E.M. Adams Co, Inc. — E.M. Adams · Class I
E.M. ADAMS CO, INC — E.M. Adams · Class I
POSEY — POSEY PRODUCTS, LLC · Class I
Restraint strap — Skytron, LLC · Class I
E.M Adams co, inc. — E.M. Adams · Class I
E.M. Adams Co, Inc. — E.M. Adams · Class I
Leg strap — Reison Medical AB · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Morrison Medical, Ltd

Sources (1)

FDA UDI 25f7b1a7-4994-4906-96e9-5bdbc0a27dde 35 fields · synced May 30, 2026