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Morrison Medical 1211RD

by Morrison Medical, Ltd

Morrison Medical 1211RD is a Class I device made by Morrison Medical, Ltd, listed in FDA GUDID since 25 Sep 2019 (UDI-DI 00647921121133), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00647921121133 UDI-DI Date25 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Morrison Medical
Generic name
Limb/torso/head restraint, reusable
Model / Ref / Catalog
1211RD
Primary DI / UDI-DI
00647921121133
FDA product code
FMQ
GMDN term
Limb/torso/head restraint, reusable
Device class
Class I
Regulation number
880.6760
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Limb/torso/head restraint, reusable

Other devices from Morrison Medical, Ltd

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Properties

  • Premarket exempt
Other properties (14, all answered No)