Aqua-Seal

Aqua-Seal Chest Drainage Unit Wet Suction, Easy-Change Connector

Registry build 21.09.26
30manufacturers in China registered for this device type
5catalogue numbers in this listing
5recalls on this code

Who Else Makes It

Concentrated in Zhejiang (8), Jiangsu (7), Guangdong (7). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GCX
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Dongguan Junhai Medical Device Co., Ltd. Dong Guang Guangdong Contract manufacturer 9
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Hospital & Homecare IMP. & EXP. Co., Ltd. Nanjing Jiangsu Contract manufacturer 179
Saferlife Products Co., Ltd. Guangzhou Guangdong Contract manufacturer 58
Gcmedica Enterprise Ltd.(Wuxi) Wuxi Jiangsu Contract manufacturer 55
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Infitek Co., Ltd. Shanghai Shanghai Manufacturer 49
Rusun Medical Co., Ltd. Yichun Jiangxi Manufacturer 37
Jiangsu JianYu Health Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 35
Tianjin Tairuibosi Medical Appliance Co., Ltd. Tianjin Tianjin Private-label distributor 30

Showing 12 of 30. All 30 manufacturers in China registered for Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Record

Regulatory record for Aqua-Seal
Listed by Cardinal Health 200, LLC, United States
FDA product code GCX
Device type Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Device class Class 2
Regulation 21 CFR 880.6740
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2025-02-18
Record revised 2025-12-31 (version 11)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Case of 5
Distribution end date 2025-12-31

Catalogue Numbers

Catalogue numbers for Aqua-Seal
Catalogue number Size Status
8888571315 In distribution
8888571299 In distribution
8888571406 In distribution
8888571315 Withdrawn
8888571406 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vacutron Allied Medical LLC 764
Cardinal Health Cardinal Health 200, LLC 310
Aesculap Aesculap AG 243
Single Use Professional Eakin Surgical Ltd 168
Medi-VAC Cardinal Health 200, LLC 158
MSI Precision Specialty Instruments MED Saver, Inc. 121
Du-O-Vac W.T. Farley, Inc. 91
Ambler Surgical Ambler Surgical, LLC 66
Apparatus, Suction, Operating-Room, Wall Vacuum Powered Biomet Microfixation 65
Wexler Surgical, Inc. Wexler Surgical, Inc. 44
OMT LLC OMT, LLC 39
Argyle Cardinal Health 38

Showing 12 of 257. All products under Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Recalls

5 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
2025-12-26 Class II Error in labeling The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older. When used on infants, the CDU may not demonstrate tidaling/bubbling, which may co 1,169,726 units
2023-12-21 Class II Process control The above-listed lots of Cardinal Health Medi-Vac CRD” Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard canister. 203244 units
2023-12-21 Class II Process control The above-listed lots of Cardinal Health Medi-Vac CRD” Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard canister. 3505730 units
2023-12-21 Class II Process control The above-listed lots of Cardinal Health Medi-Vac CRD” Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard canister. 74515
2018-03-28 Class II Process control products may be missing a one-way valve on the fluid patient port. 3600 units 2018-11-29

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