Verax Biomedical Incorporated
United States US-MF-000054515 Last updated 23 Oct 2026
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- Devices
- 15
- Registries
- GUDIDEUDAMEDFDA
- FDA recalls
- 0
Catalogue
Platelet PGDprime Controls PRM30C Ref PRM30C
Platelet PGDprime Negative Control P01113 Ref P01113
Platelet PGDprime Reagents, 20 Test PRM20R Ref PRM20R
Platelet PGDprime Positive Control P01412 Ref P01412
Platelet PGDprime Reagent 1A P01111 Ref P01111
Platelet PGDprime Processing Tubes P01462 Ref P01462
Platelet PGDprime Reagent 2 P01214 Ref P01214
Platelet PGDprime Reagents, 100 Test PRM100R Ref PRM100R
Platelet PGDprime Sample Pipettes P01230 Ref P01230
Platelet PGDprime Processing Tubes P01463 Ref P01463
Platelet PGDprime Transfer Pipettes P01229 Ref P01229
Platelet PGDprime Test T.00001186E Ref T.00001186E
Platelet PGDprime Reagent 1B P01413 Ref P01413
What Verax Biomedical Incorporated makes
Verax Biomedical Incorporated manufactures in vitro diagnostic (IVD) products focused on detecting platelet-derived growth factors (PGD) in blood samples. Their portfolio includes test kits, controls, reagents, and disposable components designed for rapid immunochromatographic testing (ICT) and clinical use, targeting platelet function analysis.
The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. Verax Biomedical Incorporated is based in the United States.
Frequently asked questions
What does Verax Biomedical Incorporated manufacture?
Verax Biomedical Incorporated manufactures in vitro diagnostic (IVD) products focused on detecting platelet-derived growth factors (PGD) in blood samples. Their portfolio includes test kits, controls, reagents, and disposable components designed for rapid immunochromatographic testing and clinical use, specifically targeting platelet function analysis.
Where is Verax Biomedical Incorporated based?
Verax Biomedical Incorporated is based in the United States. The company operates within the US, developing and manufacturing medical devices for the healthcare market.
Which regulatory registries list Verax Biomedical's devices?
Verax Biomedical's devices are listed in the FDA's Unique Device Identifier (UDI) database. This registry tracks medical devices through unique identifiers to ensure proper identification and tracking throughout their lifecycle.
How are Verax Biomedical's devices classified?
Verax Biomedical's devices are classified as Class I medical devices under FDA regulations. Class I devices are considered low-risk and subject to general controls, which include adherence to labeling, packaging, and performance standards.
Information
- Country
- United States
- Address
- 2200, West Park Drive, Westborough, MA, United States
- Website
- veraxbiomedical.com
- [email protected]
- Phone
- 1-866-948-3729
- PRRC contact
- Nancy Hornbaker
- EUDAMED SRN
- US-MF-000054515
- FDA FEI number
- 3005935106
- DUNS number
- 102312712