Accu-Chek Guide Me

Accu-Chek Guide Me Smpl Kit FC mg/dl US

Registry build 21.09.26
20manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance
5recalls on this code

Who Else Makes It

Concentrated in Guangdong (8), Jiangsu (4), Zhejiang (4). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NBW
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Sanmina Kunshan Jiangsu Contract manufacturer 15
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Flextronics Medical Device Manufacturing (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Altek Medical (kunshan) limited Kunshan Free Trade Zone Jiangsu Contract manufacturer 2
Dongguan Kaifa Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Andon Health Co., Ltd. Tianjin Tianjin Contract manufacturer 22
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21

Showing 12 of 20. All 20 manufacturers in China registered for System, Test, Blood Glucose, Over The Counter

Record

Regulatory record for Accu-Chek Guide Me
Listed by Roche Diagnostics Operations, United States
FDA product code NBW
Device type System, Test, Blood Glucose, Over The Counter
Device class Class 2
Regulation 21 CFR 862.1345
Record published 2019-04-08
Record revised 2024-12-24 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied as a kit Yes
Label carries serial number
Packaging Pack of 20, pack of 10

Catalogue Numbers

Catalogue numbers for Accu-Chek Guide Me
Catalogue number Size Status
08499918001 In distribution
08499888001 In distribution
08499896001 In distribution
08499900001 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
True Metrix Trividia Health, Inc. 40
Fora Fora Care Inc. 31
True Metrix AIR Trividia Health, Inc. 21
GE Bionime Corporation 21
TRUEtrack Trividia Health, Inc. 17
Medline Medline Industries, Inc. 15
AgaMatrix Agamatrix 15
Tenovi Tenovi Co 13
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 11
Accu-Chek Guide Roche Diagnostics Operations 10
Curaplex Bound Tree Medical, LLC 10
OneTouch Verio Lifescan Europe Gmbh 10

Showing 12 of 476. All products under System, Test, Blood Glucose, Over The Counter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K131029 2013-08-09

Recalls

3 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
2014-04-14 Class II Device Design Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips may produce erroneously low blood glucose readings in patients undergoing Ceftriaxone therapy. The interference is not described in the product labeling. 590,136 boxes 2014-09-18
2013-10-25 Class II Software design There is a software synchronization issue with the ACCU-CHEK Combo system. In rare cases, when the Manual Pump option is chosen on the ACCU-CHEK Aviva Combo meter, there is a possibility of receiving an incorrect bolus advice recommendation 6,595 units 2015-01-14
2013-03-06 Class II Device Design Roche investigation into complaints found Accu-Chek Inform II and CoaguChek XS Pro System barcode reading meters had the potential of intermittent erroneous decoding of patient identification if barcodes being read fail to meet size and/or Both devices 4467 2018-01-10
2012-03-12 Not classified Employee error Accu-Chek Aviva Nano Blood Glucose meters that were manufactured for the purpose of validating a manufacturing process for product to be distributed outside the US were distributed in the US through eBay by an unauthorized third party. The 82 meter distributed on Ebay 2012-11-06
2011-05-18 Not classified Component design/selection Erroneous results: Internal investigations revealed that the test strips exhibited a performance issue that can cause test strip errors or a bias in test result that exceed the tolerance range according to EN ISO 15197. 27,019 units 2011-10-25

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