ELANEE Vaginal-Gel (UDI 04260018197482)
Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
Device Regulatory Overview
The ELANEE Vaginal-Gel (Model/Catalog Number: ELANEE Vaginal-Gel 7 applicators DE, EN, FR, IT) 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
- ELANEE Vaginal-Gel 7 applicators DE, EN, FR, IT
- Product Code / EMDN
- U0803
- Device Name
- Żel dopochwowy/ Vaginal gel
- Database Sync Date
- 2026-08-09 16:49:19
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ELANEE Vaginal-Gel?
The registered manufacturer of record for ELANEE Vaginal-Gel is LABORATOIRE L'IDEAL Parisien Sp. z o.o..
What is the Primary UDI-DI identifier for ELANEE Vaginal-Gel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260018197482.
What classification code is assigned to this device?
This device is registered under product classification code U0803.
Similar Classification Devices (U0803)
Other Devices by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
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