GUDIDData
eudamed_udi Primary ID: 05903678429362

Jasnum gel (UDI 05903678429362)

Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Jasnum gel - Primary ID 05903678429362

Device Regulatory Overview

The Jasnum gel (Model/Catalog Number: Jasnum gel Vaginal gel 7 disposable applicators with gel and instructions for use. Polish language version.) is a medical device manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification U0803 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Jasnum gel Vaginal gel 7 disposable applicators with gel and instructions for use. Polish language version.
Product Code / EMDN
U0803
Device Name
Vaginal gel / Żel dopochwowy
Database Sync Date
2026-08-09 17:36:01

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 Jasnum gel?

The registered manufacturer of record for Jasnum gel is LABORATOIRE L'IDEAL Parisien Sp. z o.o..

What is the Primary UDI-DI identifier for Jasnum gel?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903678429362.

What classification code is assigned to this device?

This device is registered under product classification code U0803.

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