Highflow

INSUFFLATOR 45 EVAC FR 45L/MIN US version, compatible with core nova, touch screen, color display, with smoke evacuation, U: 100-240VAC, 50/60Hz, Dim. (wxhxd): 300x160x455mm

Registry build 21.09.26
10manufacturers in China registered for this device type
2catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Zhejiang (4), Guangdong (3), Jiangsu (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HIF
Manufacturer City Province Registered as Device types
Guangzhou T.K Medical Instrument Co., Ltd. Guangzhou Guangdong Contract manufacturer 7
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Scivita Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 19
Global Medical Production Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. Cixi Zhejiang Manufacturer 8
Guangdong Optomedic Technologies, Inc. Foshan Guangdong Manufacturer 7
Unimicro Medical Systems (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 6
Tianjin Uwell Medical Device Manufacturing Co Ltd Tianjin Tianjin Manufacturer 3

Record

Regulatory record for Highflow
Listed by Richard Wolf Gmbh, Germany
FDA product code HIF
Device type Insufflator, Laparoscopic
Device class Class 2
Regulation 21 CFR 884.1730
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Record published 2017-07-21
Record revised 2024-11-21 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Latex Contains natural rubber latex
Label carries manufacturing date, serial number
Storage Storage environment temperature -20 to 60 °C

Catalogue Numbers

Catalogue numbers for Highflow
Catalogue number Size Status
2235601 In distribution
2235611 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Comeg Medical Sopro 20
Insufflator, Laparoscopic Richard Wolf Gmbh 19
Airseal ConMed Corporation 10
Insufflator, Laparoscopic Smith & Nephew, Inc. 10
Gimmi Gimmi Gmbh 8
Insuflow Port Lexion Medical, LLC. 8
Aesculap Aesculap AG 7
Insufflator, Laparoscopic Stryker GmbH 6
EVA15 Palliare 6
Conmed ConMed Corporation 6
Pneumosure Stryker GmbH 6
Diversatek Healthcare Diversatek Healthcare Inc 6

Showing 12 of 114. All products under Insufflator, Laparoscopic

Recalls

2 of these are 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
2020-06-05 Class II Process control Tube material of a smaller diameter was used. 338 sets 2024-06-28
2018-03-11 Class II Use error Tube ends may be mixed up. 1710 units 2022-03-09

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