Cardinal Health

Medi Vac Yankauer Suction Handle with Tapered Bulbous Tip and Non-Conductive Suction Tubing 6 mm x 3.7 m (12 ft)

Registry build 21.09.26
70manufacturers in China registered for this device type
15catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Jiangsu (22), Zhejiang (20), Guangdong (10). 15 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JOL
Manufacturer City Province Registered as Device types
Guangzhou Nuoning Medical Supplies Co., Ltd. Guangzhou Guangdong Contract manufacturer 62
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Jiangsu JianYu Health Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 35
Ningbo Luke Medical Devices Co., Ltd. Yuyao Zhejiang Contract manufacturer 27
Primecare Medical (Suzhou) Co., Ltd. Changshu Jiangsu Contract manufacturer 20
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. Shuyang Jiangsu Contract manufacturer 18
Tylenol Medical Instruments Co., Ltd. Zhongshan Guangdong Contract manufacturer 15
VR Medical Technology Co., Ltd. Kunshan Jiangsu Contract manufacturer 13
Hangzhou Jinlin Medical Appliances Co., Ltd. Hangzhou Zhejiang Contract manufacturer 11
Ningbo Shengyurui Medical Appliance Co. Ningbo Zhejiang Contract manufacturer 11

Showing 12 of 70. All 70 manufacturers in China registered for Catheter And Tip, Suction

Record

Regulatory record for Cardinal Health
Listed by Cardinal Health 200, LLC, United States
FDA product code JOL
Device type Catheter And Tip, Suction
Device class Class 2
Regulation 21 CFR 880.6740
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-08-26
Record revised 2026-04-21 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Over the counter Yes
Supplied as a kit Yes
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date
Packaging Case of 50, case of 25, case of 40, case of 500, case of 20
Sizes Length 6 to 12 ft; lumen/inner diameter 0.24 in
Distribution end date 2028-03-31

Catalogue Numbers

Catalogue numbers for Cardinal Health
Catalogue number Size Status
KEX84 In distribution
SNE21MREUA In distribution
SID23ACSGC In distribution
KEX85 In distribution
FG71-870L In distribution
K85 Length 12 ft In distribution
K80 In distribution
KEX82 In distribution
888850970K In distribution
K83A Lumen/Inner Diameter 0.24 in In distribution
K84 Length 9 ft In distribution
KEX80 In distribution
K82 In distribution
KEX83A In distribution
SIDMVTBNMA In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Millennium Avalign Technologies, Inc. 679
Gen2 Surgix Medical LLC 497
Avalign Avalign Technologies, Inc. 459
Ambler Surgical Ambler Surgical, LLC 369
Surtex Surtex Instruments Ltd 282
Integra® Ruggles®-Redmond™ Integra LifeSciences Production Corporation 281
V. Mueller Steris Corporation 230
Liposuction Cannula Sontec Instruments, Inc. 159
Pilling Teleflex Medical LLC 135
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 127
Argyle Cardinal Health 200, LLC 125
Argyle Cardinal Health 117

Showing 12 of 397. All products under Catheter And Tip, Suction

Recalls

1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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
2023-12-04 Class I Nonconforming Material/Component Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist. 25896 units

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