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AbbVie Hip Pack 10637

by Abbvie Inc.

AbbVie Hip Pack 10637 is a Class I device made by Abbvie Inc., listed in FDA GUDID since 18 Oct 2021 (UDI-DI 08054083007953), 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 Number08054083007953 UDI-DI Date18 Oct 2021ListedStatusListed 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  • Withdrawn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
AbbVie Hip Pack
Generic name
Personal device holder, reusable
Model / reference
10637
Primary DI / UDI-DI
08054083007953
FDA product code
IQG
GMDN term
Personal device holder, reusable
Device class
Class I
Regulation number
890.5050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Personal device holder, reusable

Other devices from Abbvie Inc.

See all devices from Abbvie Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)