Evolve

EVO Bag, 500-2000ml Fill Volume, with one male luer with cap, two female luers with caps, and a needle-free injection port

Registry build 21.09.26
9manufacturers in China registered for this device type
4catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Jiangsu (5), Zhejiang (4). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KJA
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Diatrust Medical Co., Ltd. Nanjing Jiangsu Manufacturer 48
Citotest Labware Manufacturing Co., Ltd. Haimen Jiangsu Repacker / relabeller 46
Citotest Scientific Co., Ltd. Nanjing Jiangsu Repacker / relabeller 46
Trummed Medical (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 25
Zhejiang Saining Biotechnology Co., Ltd. Taizhou Zhejiang Manufacturer 12
Zhejiang Sorfa Life Science Research Co., Ltd. Hangzhou Zhejiang Contract manufacturer 9
Suzhou Cellpro Biotechnology Co., Ltd. Suzhou Jiangsu Manufacturer 6

Record

Regulatory record for Evolve
Listed by OriGen Biomedical, Inc., United States
FDA product code KJA
Device type Flask, Tissue Culture
Device class Class 1
Regulation 21 CFR 864.2240
Establishment Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-09-23
Record revised 2025-06-16 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep Dry; Special storage condition: Do not re-use; Special storage condition: Do not use if package is damaged; Special storage condition: Do not resterilize
Packaging Case of 20, case of 12
Distribution end date 2024-12-11

Catalogue Numbers

Catalogue numbers for Evolve
Catalogue number Size Status
EV120 + F-M12 In distribution
EV1000N In distribution
EV3000N In distribution
EV120 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Corning Corning Incorporated 432
Corning® PureCoat™ Corning Incorporated 20
Falcon Corning Incorporated 8
TC Flask T75,Cell+ Sarstedt Aktiengesellschaft & Co.KG 1
TC Tube 10ml 97x16PS Sarstedt Aktiengesellschaft & Co.KG 1
TC Flask T75,Stand.,Vent. Cap Sarstedt Aktiengesellschaft & Co.KG 1
PureCoat Corning Incorporated 1
TC Flask T175,Stand.,Vent. Cap Sarstedt Aktiengesellschaft & Co.KG 1
TC Tube 12ml 99x16PS Sarstedt Aktiengesellschaft & Co.KG 1
TC Flask T75,Cell+,Vented Cap Sarstedt Aktiengesellschaft & Co.KG 1
TC Flask T75,Susp.,Vent. Cap Sarstedt Aktiengesellschaft & Co.KG 1
TC Flask T25,Stand.,Vent. Cap Sarstedt Aktiengesellschaft & Co.KG 1

Showing 12 of 27. All products under Flask, Tissue Culture

Recalls

1 of these is Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2021-01-28 Class III Labeling False and Misleading It was identified that tissue culture bags were incorrectly labeled as free of phthalates. 1201 units 2023-04-19

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