LapSac

LapSac Surgical Tissue Pouch Yellow Drawstring

Registry build 21.09.26
4manufacturers in China registered for this device type
12catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Zhejiang (2), Jiangsu (1), Fujian (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KGY
Manufacturer City Province Registered as Device types
Zhejiang Aoki Medical Dressing Co., Ltd. Wenzhou Zhejiang Contract manufacturer 16
Hospital & Homecare IMP. & EXP. Co., Ltd. Nanjing Jiangsu Contract manufacturer 179
Zhejiang Mediunion Healthcare Group Co., Ltd. Ningbo Zhejiang Contract manufacturer 105
Xiamen JPL Industry & Trade Co., Ltd. Xiang An Area, Xiamen Fujian Manufacturer 2

Record

Regulatory record for LapSac
Listed by Cook Incorporated, United States
FDA product code KGY
Device type Bag, Intestine
Device class Class 1
Regulation 21 CFR 878.4100
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-10-02

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, manufacturing date
Storage Special storage condition: Store in dark, dry, cool place.

Catalogue Numbers

Catalogue numbers for LapSac
Catalogue number Size Status
G15737 In distribution
G16492 In distribution
G15738 In distribution
G15949 In distribution
G15656 In distribution
G15736 In distribution
G15883 In distribution
G16493 In distribution
G16497 In distribution
G16494 In distribution
G16495 In distribution
G16496 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Convertors Cardinal Health 200, LLC 5
LapSac Coopersurgical, Inc. 4
P&P Medical Surgical LLC P&P Medical Surgical LLC 4
Ultimate Endo retrieval pouch Purple Surgical International Limited 3
Weck Teleflex Medical LLC 3
Alleset GRI Medical & Electronic Technology Co., Ltd. 2
3M™ Steri-Drape™ 3M Company 2
Secqure Ultimate Secqure Surgical, Corp. 2
Medline-Microtek Microtek Medical LLC 2
Cardinal Health Cardinal Health 200, LLC 1
Halyard Owens & Minor Distribution, Inc. 1
Cardinal Health Microtek Medical LLC 1

Showing 12 of 20. All products under Bag, Intestine

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 Closed
2015-05-14 Class II Labeling Change Control Includes Information not stated in the intended use. 123,184 devices were distributed in commerce 2016-09-12

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