DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające (UDI 05903678429836)
Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
Device Regulatory Overview
The DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające (Model/Catalog Number: DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające 10 globules. 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 U089005 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające 10 globules. Polish language version
- Product Code / EMDN
- U089005
- Device Name
- Vaginal globules / Globulki dopochwowe
- Database Sync Date
- 2026-08-09 18:10:41
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 DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające?
The registered manufacturer of record for DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające is LABORATOIRE L'IDEAL Parisien Sp. z o.o..
What is the Primary UDI-DI identifier for DOZ PRODUCT HIALUINTIMA globulki dopochwowe nawilżające?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903678429836.
What classification code is assigned to this device?
This device is registered under product classification code U089005.
Similar Classification Devices (U089005)
Other Devices by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
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