Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013885240

FEI Number

3013885240

Entity Name

MEDKONSULT MEDICAL TECHNOLOGY S.R.O.

City/State/Country

Olomouc, CZ

Establishment Address

Pasteurova 67/15, Klasterni Hradisko, Olomouc 77900, CZ

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

MEDKONSULT medical technology s.r.o. (Owner Number: 10085039)

Owner / Operator Contact Address

Pasteurova 67/15, Klasterni Hradisko, Olomouc, CZ-712 77900, CZ

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TRYTABLE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMZ	Table, Cystometric, Electric	Gastroenterology, Urology	Class 2	876.4890	2024-11-05
FEN	Device, Cystometric, Hydraulic	Gastroenterology, Urology	Class 2	876.1620	2022-05-17
EXY	Uroflowmeter	Gastroenterology, Urology	Class 2	876.1800	2022-04-28

Official Correspondent

No official correspondent registered.

US Agent Details

Brian Hersh Business: Gemini Medical Technologies LLC Email: bhersh@geminimedtech.com Phone: (833) 9436464

Related Public Records

Same Entity

MEDKONSULT medical technology s.r.o.

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 3013885240. Last updated year: 2026. Please use registration number 3013885240 when referencing this establishment in official correspondence.