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CryoThin CS17

by Medinux (Tianjin) Technologies 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 Number06974083413412 UDI-DI Date23 Apr 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  • Withdrawn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
CryoThin
Generic Name
General cryosurgical system, cryogen gas, electronic
Model / Reference
CS17
Primary DI / UDI-DI
06974083413412
FDA Product Code
GEH
GMDN Term
General cryosurgical system, cryogen gas, electronic
Device Class
Class II
Regulation Number
878.4350
GUDID distribution status
In Commercial Distribution

Other devices from Medinux (Tianjin) Technologies Co., Ltd.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No