LABTECH KERESKEDELMI ES MERNOKI SZOLGALTATO KFT

FDA Device Registration & Listing · Debrecen Hajdu-Bihar, HU · Registration 3008799846

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
3008799846
FEI Number
3008799846
Entity Name
LABTECH KERESKEDELMI ES MERNOKI SZOLGALTATO KFT
City/State/Country
Debrecen Hajdu-Bihar, HU
Establishment Address
Vag u. 4, Debrecen Hajdu-Bihar 4031, HU
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Labtech Kereskedelmi es Mernoki Szolgaltato Kft (Owner Number: 10048231)
Owner / Operator Contact Address
Vag u. 4, Debrecen, HU-HB 4031, HU
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K140847
PMA Number
N/A

All Registered Proprietary Names

LABTECH KERESKEDELMI ES MERNOKI SZOLGALTATO KORLATOLT FELELOSSEGU TARSASAG

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MLO Electrocardiograph, Ambulatory, With Analysis Algorithm Cardiovascular Class 2 870.2800 2014-12-19

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

Labtech Kereskedelmi es Mernoki Szolgaltato Kft
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008799846. Last updated year: 2026. Please use registration number 3008799846 when referencing this establishment in official correspondence.
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