GUDIDData
eudamed_udi Primary ID: 05908226260435

HYDROVAGIN (UDI 05908226260435)

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 HYDROVAGIN - Primary ID 05908226260435

Device Regulatory Overview

The HYDROVAGIN (Model/Catalog Number: HYDROVAGIN Vaginal globules 10 globules in a single carton with instructions for use. Language version: Polish) is a medical device manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification U089005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HYDROVAGIN Vaginal globules 10 globules in a single carton with instructions for use. Language version: Polish
Product Code / EMDN
U089005
Device Name
Vaginal globules / Globulki dopochwowe
Database Sync Date
2026-08-09 16:59:16

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of HYDROVAGIN?

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

What is the Primary UDI-DI identifier for HYDROVAGIN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05908226260435.

What classification code is assigned to this device?

This device is registered under product classification code U089005.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint