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Biomed Diagnostics, Inc.

Last updated May 23, 2026

What Biomed Diagnostics, Inc. makes

Biomed Diagnostics, Inc. manufactures in vitro diagnostic culture media and identification kits, including nutrient agar, selective and differential broths, and specialized agars for detecting pathogens such as Salmonella, Staphylococcus, dermatophytes, and Candida/yeast species. Their product line includes devices like InTray® SAB, InTray® Mueller Hinton Chocolate Agar, InPouch® TV, and InTray® COLOREX Yeast, which are used for microbial culture and isolate identification in laboratory settings.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA’s 510(k) and UDI registries. Biomed Diagnostics, Inc. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Biomed Diagnostics, Inc. manufacture?

Where is Biomed Diagnostics, Inc. based?

Biomed Diagnostics, Inc. is based in the United States, as explicitly stated in the summary section of the device data.

Which regulatory registries list Biomed Diagnostics, Inc.'s devices?

Biomed Diagnostics, Inc.'s devices are listed in the FDA’s 510(k) and UDI registries, as specified in the LISTED IN field and confirmed in the summary.

How are Biomed Diagnostics, Inc.'s devices classified?

Biomed Diagnostics, Inc.'s devices are classified as Class I and Class II medical devices, as indicated in the DEVICE CLASSES field and reiterated in the summary.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
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EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (33)

Device	Model / Reference	Registries	Class	Status
QuikCoag PT-HS	10 mL	FDA UDI	Class II	Active
InTray® SAB	1263	FDA UDI	Class I	Active
QuikCoag PT-HS	2 mL	FDA UDI	Class II	Active
InTray® TSA	1443	FDA UDI	Class I	Active
InTray™ GC	1080	FDA UDI	Class II	Active
InTray® DM	2063	FDA UDI	Class I	Active
QuikCoag Control Level 3 High Abnormal	1 mL	FDA UDI	Class II	Active
QuikCoag Calcium Choride 0.02M	10 mL	FDA UDI	Class II	Active
InPouch® TV	1031	FDA UDI	Class I	Active
InTray® XLT4	1493	FDA UDI	Class I	Active
QuikCoag Control Level 1 Normal	1 mL	FDA UDI	Class II	Active
QuikCoag Calcium Chloride 0.02M	4 mL	FDA UDI	Class II	Active
InTray® COLOREX Screen	1103	FDA UDI	Class I	Active
InPouch® TVC Subculture	1051	FDA UDI	Class I	Active
InTray® Mueller Hinton Chocolate Agar	2483	FDA UDI	Class I	Active
InTray® Brilliant Green	1463	FDA UDI	Class I	Active
InTray® COLOREX Yeast	1113	FDA UDI	Class I	Active
QuikCoag Control Level 2 Low Abnormal	1 mL	FDA UDI	Class II	Active
QuikCoag PT-HS	4 mL	FDA UDI	Class II	Active
InTray® SAB+PVG	2127	FDA UDI	Class I	Active
QuikCoag APTT-EA	10 mL	FDA UDI	Class II	Active
InTray® Malt Extract Agar	1333	FDA UDI	Class I	Active
Saline Solution (0.85%)	1612	FDA UDI	Class I	Active
InTray® COLOREX Salmonella	1223	FDA UDI	Class I	Active
QuikCoag APTT-EA	4 mL	FDA UDI	Class II	Active
InTray® MSA	1303	FDA UDI	Class I	Active
InTray® PDA	1293	FDA UDI	Class I	Active
VTM-C19 Transit Tube	1602	FDA UDI	Class I	Active
InTray® SMA	1423	FDA UDI	Class I	Active
InTray® BHI	1503	FDA UDI	Class I	Active
InTray DM-FungID	1593	FDA UDI	Class I	Active
Inpouch-Tv Pouch	K896296	FDA 510(k)	Class I	Active
Intray Gc	K993033	FDA 510(k)	Class II	Active

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