Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017871324

FEI Number

3017871324

Entity Name

HIMEDIA LABORATORIES PRIVATE LIMITED

City/State/Country

Thane Maharashtra, IN

Establishment Address

E51 Plant, Additional Ambernath MIDC, Anand Nagar, Ambernath (East), Thane Maharashtra 421506, IN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

HiMedia Laboratories Private Limited (Owner Number: 10079743)

Owner / Operator Contact Address

C40 Road No. 21 Y, MIDC, Wagle Industrial Area, Thane, IN-MH 400604, IN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CV and NaCL Plate Ready Prepared Plates (MP081 MacConkey Agar w/ 0.15% Bile Salts Ready Prepared Plates (MP096 Potato Dextrose Agar Plate) Ready Prepared Plates-Mueller Hinton Agar (MP173) Ready Prepared Plates (MP1353 HiCrome UTI Agar Plate)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JSI	Culture Media, Selective And Differential	Microbiology	Class 1	866.2360	2021-04-22
JSG	Culture Media, Non-Selective And Non-Differential	Microbiology	Class 1	866.2300	2021-04-22
JSJ	Culture Media, Selective And Non-Differential	Microbiology	Class 1	866.2360	2021-04-22
JSA	Culture Media, Antibiotic Assay	Microbiology	Class 1	866.2350	2020-12-21
JSH	Culture Media, Non-Selective And Differential	Microbiology	Class 1	866.2320	2021-04-22

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

HiMedia Laboratories Private Limited

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K862389	Otisville Biotech, Inc.	BIOTIS ACETAMIDE AGAR	1986-07-03
K811644	Hardy Media	HEKTOEN ENTERIC AGAR	1981-07-02
K832535	Otisville Biotech, Inc.	HEKTOEN ENTERIC AGAR PLATE	1983-10-04
K811331	Acumedia Manufacturers, Inc.	SF BROTH	1981-05-29
K872058	Orion Corp.	ORICULT-N CULTURE-PADDLE	1987-06-10

Similar Registrations

Registration Number	Establishment Name	Location
9680687	CHROMAGAR	Saint-Denis Seine-Saint-Denis, FR
3005182159	HIMEDIA LABORATORIES PRIVATE LIMITED	NASHIK Maharashtra, IN
2016672	KEY SCIENTIFIC PRODUCTS	Stamford, TX, US
3033815621	GUANGDONG HUANKAI BIOLOGY SCI.&TECH.CO.,LTD	Zhaoqing Guangdong, CN
8023060	BIO-RAD	STEENVOORDE Nord, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017871324. Last updated year: 2026. Please use registration number 3017871324 when referencing this establishment in official correspondence.