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Dr. Aktive A02-C-032-E1

by Chengdu Cryo-push Medical Technology 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 Number06973641880680 UDI-DI Date21 Jul 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  • Withdrawn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
Dr. Aktive
Generic Name
Circulating-fluid localized thermal/compression therapy system wrap
Model / Reference
A02-C-032-E1
Primary DI / UDI-DI
06973641880680
FDA Product Code
IRP, ILO
GMDN Term
Circulating-fluid localized thermal/compression therapy system wrap
Device Class
Class II
Regulation Number
890.5650, 890.5720
GUDID distribution status
In Commercial Distribution

Other devices from Chengdu Cryo-push Medical Technology Co., Ltd.

See all devices from Chengdu Cryo-push Medical Technology Co., Ltd. →

Properties

  • Lot / Batch Number
  • Manufacturing Date

Other properties (12)

  • 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
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No