Monitect Drug Screen Cassette Test

OPI2000/MET1000/THC50/COC300 Cassette Tests with Adulteration Screen for OX-PH-CR-NI

Registry build 21.09.26
16manufacturers in China registered for this device type
9catalogue numbers in this listing
5510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Zhejiang (9), Guangdong (3), Beijing (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DIO
Manufacturer City Province Registered as Device types
Hangzhou Biotest Biotech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 41
Abon Biopharm (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 17
Core Technology Co., Ltd. Changping District Beijing Contract manufacturer 14
Prometheus Bio Inc. Hangzhou Zhejiang Contract manufacturer 12
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Hangzhou AllTest Biotech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 48
Assure Tech. (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 48
Guangzhou Wondfo Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 44
W.h.p.m. Bioresearch & Technology Co., Ltd. Beijing Beijing Manufacturer 37
Guangzhou Decheng Biotechnology Co., Ltd. Guangzhou Guangdong Complaint-file establishment 35
Changchun Wancheng BIO-Electron Co., Ltd. Changchun Jilin Contract manufacturer 34
Co-Innovation Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 29

Showing 12 of 16. All 16 manufacturers in China registered for Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Record

Regulatory record for Monitect Drug Screen Cassette Test
Listed by Branan Medical Corporation, United States
FDA product code DIO
Device type Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Device class Class 2
Regulation 21 CFR 862.3250
510(k) K004034
Record published 2016-08-01
Record revised 2022-06-10 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 15 to 30 °C
Distribution end date 2018-11-02

Catalogue Numbers

Catalogue numbers for Monitect Drug Screen Cassette Test
Catalogue number Size Status
TC19 Withdrawn
TC11A Withdrawn
BC10A Withdrawn
BC10 Withdrawn
TC11 Withdrawn
MC11 Withdrawn
TC13 Withdrawn
QC12A Withdrawn
QC12 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Healgen Healgen Scientific Limited Liability Company 19
iCup® Instant Technologies, Inc. 15
DrugCheck Express Diagnostics Int’l., Inc. 12
AlereTM iScreen® Instant Technologies, Inc. 9
MD DugScreen Medical Disposables Corp 9
First Sign® Hemosure Inc. 8
Rapid Response Btnx Inc. 7
Identify® Diagnostics Drug Test Cards Medical Distribution Group Inc 7
iScreen™ Instant Technologies, Inc. 7
SureStep™ Urine Test E-Z Split Key™ Drug Screen Cup Alere San Diego, Inc. 7
DrugCheck Express Diagnostic Int’l, Inc. 7
Enzyme Immunoassay, Cocaine And Cocaine Metabolites W.h.p.m., Inc. 7

Showing 12 of 152. All products under Enzyme Immunoassay, Cocaine And Cocaine Metabolites

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K103227 2012-04-11
K032057 2003-08-21
K023489 2002-12-16
K022355 2002-07-30
K002264 2000-11-27

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2016-07-05 Class III Labeling mix-ups Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug cup, because it may erroneously contain 12 panel cups due to a packaging error. 96 units 2016-10-04
2014-03-26 Class II Labeling Change Control May be labeled with incorrect result interpretation graphics on the ToxCup lid label. 9,800 units 2014-07-23

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