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magicgel Migraineicepack2PK

by Anhui Kamt Ice Pack Co., Ltd.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06975306620051 UDI-DI Date25 Oct 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
magicgel
Generic Name
Musculoskeletal hot/cold therapy pack, reusable
Model / Reference
Migraineicepack2PK
Primary DI / UDI-DI
06975306620051
FDA Product Code
KYR
GMDN Term
Musculoskeletal hot/cold therapy pack, reusable
Device Class
Class I
Regulation Number
880.6050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hot/cold therapy pack, reusable

Other devices from Anhui Kamt Ice Pack Co., Ltd.

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No