Accessories, Germicide, Cleaning, for Endoscopes

The Flow Units are accessories that facilitate use of the Reliance EPS processor with specific endoscopes and endoscope accessory parts.

Registry build 21.09.26
1manufacturer
11catalogue numbers in this listing

Who Else Makes It

Registered in Zhejiang. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NZA
Manufacturer City Province Registered as Device types
Saint-Gobain Life Sciences (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 5

Record

Regulatory record for Accessories, Germicide, Cleaning, For Endoscopes
Listed by Corporation Steris Canada
FDA product code NZA
Device type Accessories, Germicide, Cleaning, For Endoscopes
Device class Class 2
Regulation 21 CFR 876.1500
510(k) K040049
Record published 2016-09-13
Record revised 2025-06-12 (version 12)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Label carries lot or batch number
Distribution end date 2025-06-11

Catalogue Numbers

Catalogue numbers for Accessories, Germicide, Cleaning, For Endoscopes
Catalogue number Size Status
Flow Unit 3 In distribution
Flow Unit 1 In distribution
Flow Unit 2 In distribution
Flow Unit 7 In distribution
Flow Unit 6 In distribution
Flow Unit 4 In distribution
Flow Unit 5 Withdrawn
Flow Unit 11 Withdrawn
Flow Unit 9 Withdrawn
Flow Unit 8 Withdrawn
Flow Unit 10 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Reliance Corporation Steris Canada 6
Accessories, Germicide, Cleaning, For Endoscopes Pentax of America, Inc. 2
Reliance Steris Corporation 1

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Accessories, Germicide, Cleaning, For Endoscopes
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Steris Corporation 510(k) number 2013-08-29 Class II Use error The air pipe that delivers unfiltered ambient air from the procedure room into the water bottle on the listed FUJINON G5 & G8 type flexible GI endoscopes does not connect to the main air/water channel within the light guide (LG) connection 266 units 2014-07-03

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