Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003995437

FEI Number

3003995437

Entity Name

TECHNIDATA

City/State/Country

MONTBONNOT ST. MARTIN Isere, FR

Establishment Address

387, AVENUE JEAN KUNTZMANN, MONTBONNOT ST. MARTIN Isere 38330, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

TECHNIDATA SAS (Owner Number: 9048182)

Owner / Operator Contact Address

387, AVENUE JEAN KUNTZMANN, --, MONTBONNOT ST MARTIN, FR-NOTA 38330, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TD BactiLink TD NexLabs TD-GENET TDHISTO/CYTO TDMind TD-SYNERGY TD-MICRO TDCONCENTRATOR TD-WEB TD-MIDDLEWARE TDWORKSTATION

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JQP	Calculator/Data Processing Module, For Clinical Use	Clinical Chemistry	Class 1	862.2100	2003-03-21

Official Correspondent

No official correspondent registered.

US Agent Details

MINDY McCANN Business: Qserve Group US Inc. Email: USagent@qservegroup.com Phone: (215) 6003103

Related Public Records

Same Entity

TECHNIDATA SAS

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
K781173	Instrumentation Laboratory CO	COMPUTER INTERFACE IL 814	1978-09-14

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-04	Misys Healthcare Systems	1	Calculator/Data Processing Module for Clinical Use
Z-0026-2025	Becton Dickinson & Co.	1	BD Synapsys Informatics Solution with software versions: 4.20, 4.30, 5.10, 5.20 and 5.30- IVD standalone laboratory software solution providing data management and workflow management functionality across locations where clinical diagnostic activities take place. Catalog Number: 444150

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3015426626	Aclarion, Inc.	Broomfield, CO, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003995437. Last updated year: 2026. Please use registration number 3003995437 when referencing this establishment in official correspondence.