Accu-Chek Spirit Cartridge

Accu-Chek Spirit 3.15ml Cart. Sys. 5pcs

Registry build 21.09.26
7manufacturers in China registered for this device type
2catalogue numbers in this listing
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Guangdong (3), Shanghai (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LZG
Manufacturer City Province Registered as Device types
Sanmina Kunshan Jiangsu Contract manufacturer 15
Providence Enterprise Limited Shenzhen Guangdong Contract manufacturer 9
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Advance Technology Ltd Shenzhen Guangdong Contract manufacturer 3
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Viant Medical Suzhou EPZ Co., Ltd. Jiangsu Jiangsu Contract manufacturer 3

Record

Regulatory record for Accu-Chek Spirit Cartridge
Listed by Roche Diabetes Care, Inc., United States
FDA product code LZG
Device type Pump, Infusion, Insulin
Device class Class 2
Regulation 21 CFR 880.5725
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K042887
Record published 2016-08-26
Record revised 2023-07-25 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Distribution end date 2022-12-15

Catalogue Numbers

Catalogue numbers for Accu-Chek Spirit Cartridge
Catalogue number Size Per pack Status
04949935001 5 Withdrawn
05206073001 25 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OneTouch Ping Animas Corp. 12
Easy Release Sooil Development Co., Ltd. 9
V-Go Disposable Insulin Delivery Mannkind Corporation 6
Accu-Chek Combo Roche Diabetes Care, Inc. 5
Superline Sooil Development Co., Ltd. 4
t:slim Cartridge, t:lock, 10 Pack Tandem Diabetes Care, Inc. 3
Dana Diabecare Sooil Development Co., Ltd. 3
t:slim X2 Insulin Pump Tandem Diabetes Care, Inc. 2
Omnipod Insulet Corporation 2
Soft-Release-ST Sooil Development Co., Ltd. 2
t:slim Insulin Pump, Replacement Tandem Diabetes Care, Inc. 1
MODD1 Infusion Set, 10 Pack Modular Medical 1

Showing 12 of 53. All products under Pump, Infusion, Insulin

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Accu-Chek Spirit Cartridge
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Roche Diabetes Care, Inc. 510(k) number 2015-04-22 Class II Device Design Roche has become aware of an increase of mechanical errors experienced by customers using the Accu-Chek Spirit Combo insulin infusion pump and Accu-Chek Spirit insulin infusion pump when the insulin pumps display E6 and El0 error messages. 35,795 2016-11-03

Recalls

2 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
2021-07-28 Class II Package design/selection Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decis 10,546,420 (US), 19,120,668 (OUS)
2015-04-22 Class II Device Design Roche has become aware of an increase of mechanical errors experienced by customers using the Accu-Chek Spirit Combo insulin infusion pump and Accu-Chek Spirit insulin infusion pump when the insulin pumps display E6 and El0 error messages. 35,795 2016-11-03

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