Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003615065

FEI Number

3003615065

Entity Name

MAQUILAS TETA KAWI S.A. DE C.V.

City/State/Country

NOGALES KM2 EMPALME Sonora, MX

Establishment Address

CARRETERA INTL. KM. 1969, GUADALAJARA, NOGALES KM2 EMPALME Sonora 85340, MX

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Precision Interconnect, LLC (Owner Number: 9060212)

Owner / Operator Contact Address

10025 SW Freeman Ct, Wilsonville, OR 97070, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MARQUETTE SV O2 MODULE ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DQE	Catheter, Oximeter, Fiber-Optic	Cardiovascular	Class 2	870.1230	2016-09-22
LDD	Dc-Defibrillator, Low-Energy, (Including Paddles)	Cardiovascular	Class 2	870.5300	2014-09-05

Official Correspondent

No official correspondent registered.

US Agent Details

Tafzeelur Rahaman Email: Tafzeelur.rahaman@te.com Phone: (408) 8564459

Related Public Records

Same Entity

Precision Interconnect, LLC

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
K203231	Philips North America, LLC	Switched Internal Paddles	2021-01-11
K200849	Remote Diagnostic Technologies, Ltd. A Philips Company	Tempus LS - Manual	2020-07-24

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0557-2025	Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom	2	Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
Z-0564-2021	Remote Diagnostic Technologies Ltd. PAVILION C2, ASHWOOD PARK ASHWOOD WAY Basingstoke United Kingdom	2	Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in the following environmental: - Primarily in pre-hospital care and transport applications (including ambulances, fixed and rotary wing aircraft).
Z-0861-2022	Remote Diagnostic Technologies Ltd. PAVILION C2, ASHWOOD PARK ASHWOOD WAY Basingstoke United Kingdom	2	Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693
Z-1825-2023	Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom	2	Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Z-2028-2024	Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom	2	Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual

Similar Registrations

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3006082230	C.R. BARD, INC.	MADISON, GA, US
3032916632	BECTON, DICKINSON AND COMPANY	Irvine, CA, US
3013319212	ICU MEDICAL, INC.	Lake Forest, IL, US
1720929	ISOMEDIX OPERATIONS INC.	Sandy, UT, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003615065. Last updated year: 2026. Please use registration number 3003615065 when referencing this establishment in official correspondence.