Tube Set Adapter

Two spike ports to one spike with 16cm SCD tubing

Registry build 21.09.26
12manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Jiangsu (6), Zhejiang (5), Liaoning (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KJG
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Jiangsu Kangjian Medical Apparatus Co., Ltd. Jiangyan Jiangsu Contract manufacturer 19
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Huzhou Junda Industry Co., Ltd. Anji Zhejiang Contract manufacturer 129
Zhejiang Lidesen Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 100
Anji Spenq Industrial Co., Ltd. Huzhou Zhejiang Manufacturer 85
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
Dalian Rongbang Medical Healthy Devices Co Ltd Dalian Liaoning Contract manufacturer 15
Suzhou Cnnc Huadong Radiation Co., Ltd. Suzhou Jiangsu Contract manufacturer 12
Zhejiang Saining Biotechnology Co., Ltd. Taizhou Zhejiang Manufacturer 12

Record

Regulatory record for Tube Set Adapter
Listed by OriGen Biomedical, Inc., United States
FDA product code KJG
Device type Tube, Tissue Culture
Device class Class 1
Regulation 21 CFR 864.3010
Establishment Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-09-23
Record revised 2025-06-18 (version 3)

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
Packaging Case of 20

Catalogue Numbers

Catalogue numbers for Tube Set Adapter
Catalogue number Size Status
2P-S16 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Bioseal Inc. Bioseal 32
Accessories OriGen Biomedical, Inc. 18
Spike Adapter OriGen Biomedical, Inc. 14
Custom Healthcare Systems Inc. Manus Medical, LLC 9
LabChoice Culture Tubes, With Dual Position Cap, Polystyrene, 17 x 100 mm Dynarex Corp. 7
TubeSet Adapter OriGen Biomedical, Inc. 5
Cardinal Health Cardinal Health 200, LLC 5
Injection Spike OriGen Biomedical, Inc. 3
Accessory Sets OriGen Biomedical, Inc. 3
Accessory Set OriGen Biomedical, Inc. 3
Female to Female Adapter OriGen Biomedical, Inc. 2
3ml Syringe, FLL X SCD OriGen Biomedical, Inc. 2

Showing 12 of 51. All products under Tube, Tissue Culture

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
2023-12-19 Class II Nonconforming Material/Component Accessory sets contain a syringes not yet qualified for the accessory’s intended purpose; due to design changes to the syringe barrels and a polypropylene resin change that resulted in loss of gamma compatibility, for accessory set syringes 3613 Cases

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