Wallach Cryosurgical Equipment

WALLACH Cryosurgical Equipment UltraFreeze Liquid Nitrogen Sprayer (.5 liter)

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
16recalls on this code

Who Else Makes It

Concentrated in Guangdong (1), Beijing (1), Tianjin (1).

Chinese manufacturers registered for FDA product code GEH
Manufacturer City Province Registered as Device types
Shenzhen Kesite Digital Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Hygea Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2
Medinux (Tianjin) Technologies Co., Ltd. Tianjin Tianjin Manufacturer 1

Record

Regulatory record for Wallach Cryosurgical Equipment
Listed by Coopersurgical, Inc., United States
FDA product code GEH
Device type Unit, Cryosurgical, Accessories
Device class Class 2
Regulation 21 CFR 878.4350
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K935010
Record published 2016-10-26
Record revised 2024-02-28 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries serial number

Catalogue Numbers

Catalogue numbers for Wallach Cryosurgical Equipment
Catalogue number Size Status
900076 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Frigitronics Coopersurgical, Inc. 42
CryoProbe™ H&O Equipments, Nv/Sa 35
Wallach Coopersurgical, Inc. 32
Premier Premier Dental Products Co. 30
Hygea Hygea Medical Technology Co., Ltd. 26
truFreeze CSA Medical 20
Freezpen® H&O Equipments, Nv/Sa 19
Leisegang Cryotip for LM-900 Coopersurgical, Inc. 15
Integra® Miltex® Integra LifeSciences Production Corporation 13
cryoICE Cryoablation System Atricure, Inc. 13
CryoThin Medinux (Tianjin) Technologies Co., Ltd. 12
Erbe Erbe Elektromedizin GmbH 12

Showing 12 of 334. All products under Unit, Cryosurgical, Accessories

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2015-03-09 Class II Under Investigation by firm Internal gas line may malfunction causing the line to burst under pressure. 255 units 2016-02-01
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 3,044 units 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2009-09-29 Not classified Device Design CO2 Cryosystem thermal load may exceed the exhaust gas phase, resulting in ice formation in the exhaust valve. Should this occur, the Cryo tip may cool at a less than optimal rate, resulting in ice formation in the exhaust valve. 2012-04-17
2007-06-06 Not classified Device Design The tip may separate from the probe. 315 units 2015-07-15
2007-06-06 Not classified Device Design The tip may separate from the probe. 14 units 2015-07-15

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

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