FOMUKAL (UDI 05901812160645)
Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
Device Regulatory Overview
The FOMUKAL (Model/Catalog Number: FOMUKAL płyn do płukania jamy ustnej 2A+2B – czteropak, wersja 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 V9017 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FOMUKAL płyn do płukania jamy ustnej 2A+2B – czteropak, wersja polska
- Product Code / EMDN
- V9017
- Device Name
- FOMUKAL płyn do płukania jamy ustnej
- Database Sync Date
- 2026-08-09 16:48:07
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 FOMUKAL?
The registered manufacturer of record for FOMUKAL is LABORATOIRE L'IDEAL Parisien Sp. z o.o..
What is the Primary UDI-DI identifier for FOMUKAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901812160645.
What classification code is assigned to this device?
This device is registered under product classification code V9017.
Similar Classification Devices (V9017)
Other Devices by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
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