Plastic Electromechanic Company Plus

FDA Device Registration & Listing · Z.I HAMMAM-ZRIBA Zaghouan, TN · Registration 3014982336

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
3014982336
FEI Number
3014982336
Entity Name
Plastic Electromechanic Company Plus
City/State/Country
Z.I HAMMAM-ZRIBA Zaghouan, TN
Establishment Address
Z.I Hammam-Zriba BP 226 Hammam-Zriba 1152 ZAGHOUAN TUNISIE (PEC PLUS), Z.I HAMMAM-ZRIBA Zaghouan 1152, TN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PLastic Electromechanic company PLUS (Owner Number: 10058990)
Owner / Operator Contact Address
32, 33 ZI Hammam Zriba BP34 1152, Hammam Zriba, TN-22 1152, TN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Electrode, electrocardiograph

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRX Electrode, Electrocardiograph Cardiovascular Class 2 870.2360 2018-11-19
DSA Cable, Transducer And Electrode, Patient, (Including Connector) Cardiovascular Class 2 870.2900 2024-07-30

Official Correspondent

Slim Jebri

US Agent Details

Jessica Potter Business: GRAPHIC CONTROLS d.b.a Nissha Medical Technologies Email: jpotter@nisshamedical.com Phone: (716) 8496367

Related Public Records

Same Entity

PLastic Electromechanic company PLUS
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
K934333 3M Medical Products Group 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE 1994-07-07
K880323 Medtronic Vascular MEDTRONIC MODEL 5411 SURGICAL CABLE ADAPTOR 1988-03-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014982336. Last updated year: 2026. Please use registration number 3014982336 when referencing this establishment in official correspondence.
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