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cryoICE® System A001150

by Atricure, Inc. 8 variants

cryoICE® System A001150 (A001150-3) is a Class II device made by Atricure, Inc., listed in FDA GUDID since 27 May 2026 (UDI-DI 10840143902680), 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 Number10840143902680 UDI-DI Date27 May 2026ListedStatusListed 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  • Withdrawn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
cryoICE® System
Generic name
General cryosurgical system, cryogen gas, mechanical
Model / Ref / Catalog
A001150, A001150-3
Primary DI / UDI-DI
10840143902680
FDA product code
GEH
GMDN term
General cryosurgical system, cryogen gas, mechanical
Device class
Class II
Regulation number
878.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
High-level Disinfectant

Other devices from Atricure, Inc.

See all devices from Atricure, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)