DOZ MED HIALUINTIMA GLOBULKI DOPOCHWOWE (UDI 05906122471382)
Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
Device Regulatory Overview
The DOZ MED HIALUINTIMA GLOBULKI DOPOCHWOWE (Model/Catalog Number: DOZ MED HIALUINTIMA GLOBULKI DOPOCHWOWE 10 globulek w kartoniku z instrukcją używania. Wersja językowa polska.) 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 MED HIALUINTIMA GLOBULKI DOPOCHWOWE 10 globulek w kartoniku z instrukcją używania. Wersja językowa polska.
- Product Code / EMDN
- U089005
- Device Name
- Globulki dopochwowe/ Vaginal globules
- Database Sync Date
- 2026-08-09 18:15:01
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 MED HIALUINTIMA GLOBULKI DOPOCHWOWE?
The registered manufacturer of record for DOZ MED HIALUINTIMA GLOBULKI DOPOCHWOWE is LABORATOIRE L'IDEAL Parisien Sp. z o.o..
What is the Primary UDI-DI identifier for DOZ MED HIALUINTIMA GLOBULKI DOPOCHWOWE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05906122471382.
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.
Programmatic Export
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