Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010386080

FEI Number

3010386080

Entity Name

SIA ELMI

City/State/Country

Riga, Latvia, LV

Establishment Address

Bukultu 7b, Riga, Latvia LV-1005, LV

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SIA ELMI (Owner Number: 10043759)

Owner / Operator Contact Address

D. Brantkalna 3-38, Riga, LV-RIX LV-1005, LV

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JQC	Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use	Clinical Chemistry	Class 1	862.2050	2013-03-20

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

SIA ELMI

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010386080. Last updated year: 2026. Please use registration number 3010386080 when referencing this establishment in official correspondence.