GUDIDData
eudamed_udi Primary ID: 06192491101916

Jersey tubulaire Hydrofuge 7cmx25 m Côtelé en Sachet (UDI 06192491101916)

Manufactured by Plastic Electromechanic Company Medical International

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Jersey tubulaire Hydrofuge 7cmx25 m Côtelé en Sachet - Primary ID 06192491101916

Device Regulatory Overview

The Jersey tubulaire Hydrofuge 7cmx25 m Côtelé en Sachet (Model/Catalog Number: 206000CF5-25M/S) is a medical device manufactured by Plastic Electromechanic Company Medical International. This product is indexed under FDA Product Code / Category Classification M03030202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
206000CF5-25M/S
Product Code / EMDN
M03030202
Device Name
TUBINET
Database Sync Date
2026-08-09 16:49:42

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Jersey tubulaire Hydrofuge 7cmx25 m Côtelé en Sachet?

The registered manufacturer of record for Jersey tubulaire Hydrofuge 7cmx25 m Côtelé en Sachet is Plastic Electromechanic Company Medical International.

What is the Primary UDI-DI identifier for Jersey tubulaire Hydrofuge 7cmx25 m Côtelé en Sachet?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06192491101916.

What classification code is assigned to this device?

This device is registered under product classification code M03030202.

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