WEIDMANN TECNOLOGIA ELECTRICA DE MEXICO S.A. DE C.V.

FDA Device Registration & Listing · Arteaga Coahuila, MX · Registration 3013267051

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
3013267051
FEI Number
3013267051
Entity Name
WEIDMANN TECNOLOGIA ELECTRICA DE MEXICO S.A. DE C.V.
City/State/Country
Arteaga Coahuila, MX
Establishment Address
Carr. Lib. Prof. Oscar Flores Tapia No. 304. Col. El Llano, Arteaga Coahuila 25350, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Weidmann Tecnologia Electrica de Mexico S.A. de C.V. (Owner Number: 10079866)
Owner / Operator Contact Address
Carr. Lib. Prof. Oscar Flores Tapia No. 304. Col. El Llano, Arteaga, MX-COA 25350, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

cobas omni ProcessingPlate

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2020-12-29

Official Correspondent

Erendira Garza

US Agent Details

Jill O'Neal Business: Weidmann Electrical Technology Inc Email: jill.oneal@weidmann-group.com Phone: (937) 5082106

Related Public Records

Same Entity

Weidmann Tecnologia Electrica de Mexico S.A. de C.V.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013267051. Last updated year: 2026. Please use registration number 3013267051 when referencing this establishment in official correspondence.
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