Torrent and AquaShield

Torrent and AquaShield System Kit (ERBE Byrne)

Registry build 21.09.26
4manufacturers in China registered for this device type
2catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FEQ
Manufacturer City Province Registered as Device types
Jiangsu JianYu Health Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 35
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24

Record

Regulatory record for Torrent and AquaShield
Listed by Us Endoscopy, United States
FDA product code FEQ
Device type Pump, Air, Non-Manual, For Endoscope
Device class Class 2
Regulation 21 CFR 876.1500
Record published 2016-09-17
Record revised 2022-06-10 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number
Storage Storage environment temperature 15 to 25 °C
Distribution end date 2019-03-25

Catalogue Numbers

Catalogue numbers for Torrent and AquaShield
Catalogue number Size Status
00711545 Withdrawn
00711544 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Erbe Erbe Elektromedizin GmbH 24
AquaShield Us Endoscopy 16
Olympus Keymed (Medical & Industrial Equipment) Ltd 13
Hydra Boston Scientific Corporation 13
Erbeflo CleverCap® Erbe Medical, LLC 8
Olympus Olympus Winter & IBE Gmbh 7
Erbeflo AeroRinse® Erbe Medical, LLC 4
Endogator Medivators Inc 4
Defendo Medivators Inc 3
CS-05-00-290 OpClear Disposable Cipher Surgical Ltd 1
CS-10-00-300 OpClear Disposable Cipher Surgical Ltd 1
CS-10-00-315 OpClear Disposable Cipher Surgical Ltd 1

Showing 12 of 30. All products under Pump, Air, Non-Manual, For Endoscope

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer