Hema-Screen ER Developer

Catalogue number HSDVER-8, listed by Immunostics, Inc., United States, under Reagent, Occult Blood. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (1), Beijing (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KHE
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Hangzhou Genesis Biodetection & Biocontrol Co., Ltd. Hangzhou Zhejiang Contract manufacturer 5
Guangzhou Wondfo Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 44
W.h.p.m. Bioresearch & Technology Co., Ltd. Beijing Beijing Manufacturer 37
Chong Qing Teco Huayi Pharm. Co. Shapingba Dist. Chongqing Contract manufacturer 18

Record

Regulatory record for hema-screen ER developer
Listed by Immunostics, Inc., United States
FDA product code KHE
Device type Reagent, Occult Blood
Device class Class 2
Regulation 21 CFR 864.6550
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-23
Record revised 2025-03-31 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 15 to 30 °C
Packaging Case of 10 of 10

Catalogue Numbers

Catalogue numbers for hema-screen ER developer
Catalogue number Size Per pack Status
HSDVER-8 8 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OC-Light S Polymedco Cancer Diagnostic Products LLC 59
McKesson Mckesson Medical-Surgical Inc. 21
Hemosure Hemosure Inc. 21
Hemoccult Beckman Coulter, Inc. 17
Henry Schein Henry Schein, Inc. 14
PremierPro Prestige Ameritech 11
hema-screen Specific Immunostics, Inc. 9
InSure® ONE™ Enterix Inc. 8
InSure FIT Enterix Inc. 7
hema-screen Immunostics, Inc. 7
ADS Medical W.h.p.m., Inc. 7
QuickVue Quidel Corp. 6

Showing 12 of 135. All products under Reagent, Occult Blood

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K171484 2017-06-14
K163554 2017-01-17
K102664 2011-01-28
K060463 2006-06-06
K992759 1999-12-06
K902360 1990-07-27
K854619 1986-03-03

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