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Procare 79-91645

by Djo, LLC

Procare 79-91645 is a Class I device made by Djo, LLC, listed in FDA GUDID since 1 Dec 2022 (UDI-DI 00888912038805), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888912038805 UDI-DI Date1 Dec 2022ListedStatusListed 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  • Withdrawn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
Procare
Generic name
Wheelchair/chair/stander occupant restraint/support
Model / reference
79-91645
Primary DI / UDI-DI
00888912038805
FDA product code
FMQ
GMDN term
Wheelchair/chair/stander occupant restraint/support
Device class
Class I
Regulation number
880.6760
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wheelchair/chair/stander occupant restraint/support

Similar devices in this category

Other devices filed under Wheelchair/chair/stander occupant restraint/support.

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

  • Prescription use
  • Manufacturing date
Other properties (13, all answered No)