ELITechGroup MICROBIO

FDA Device Registration & Listing · SIGNES Var, FR · Registration 3006091463

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006091463
FEI Number
3006091463
Entity Name
ELITechGroup MICROBIO
City/State/Country
SIGNES Var, FR
Establishment Address
Parc d activites du plateau, 19, allee d Athenes, SIGNES Var 83870, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ELITechGroup Inc. (Owner Number: 1717966)
Owner / Operator Contact Address
370 West 1700 South, Logan, UT 84321, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Serology Reference 00014 Mycoplasma Stabilizer REF 00064 MYCOFAST US Mycofast US: Ref 00050 Mycoplasma Control: ref 00900

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GSA Antisera, All Mycoplasma Spp. Microbiology Class 1 866.3375 2009-04-24
JSK Supplement, Culture Media Microbiology Class 1 866.2450 2011-07-28
JTO Discs, Strips And Reagents, Microorganism Differentiation Microbiology Class 1 866.2660 2009-04-24
JTR Kit, Quality Control For Culture Media Microbiology Class 1 866.2480 2011-07-28

Official Correspondent

No official correspondent registered.

US Agent Details

Robert Ortiz Business: ELITechGroup Inc. Email: robert.ortiz@elitechgroup.com Phone: (435) 7526011

Related Public Records

Same Entity

ELITechGroup Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3044320359 ELITechGroup Inc., Tucson Tucson, AZ, US
3011461582 ELITechGroup S.p.A. Torino Piedmont, IT
3003540236 ELITechGroup MDX LLC. Bothell, WA, US
1717966 ELITechGroup Inc LOGAN, UT, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K770926 Analytical Products, Inc. SUSPENSION SALINE, API 20E 1977-06-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006091463. Last updated year: 2026. Please use registration number 3006091463 when referencing this establishment in official correspondence.
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