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Guanyin ICE001

by Shanghai Guanyin 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971898341237 UDI-DI Date7 Sep 2026ListedStatusListed 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  • Withdrawn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
Guanyin
Generic Name
Musculoskeletal hot/cold therapy pack, single-use
Model / Reference
ICE001
Primary DI / UDI-DI
06971898341237
FDA Product Code
IMD
GMDN Term
Musculoskeletal hot/cold therapy pack, single-use
Device Class
Class I
Regulation Number
890.5710
GUDID distribution status
In Commercial Distribution

Other devices from Shanghai Guanyin 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