eudamed_udi
Primary ID: 05903260909470
BliznOFF (UDI 05903260909470)
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 BliznOFF - Primary ID 05903260909470
Device Regulatory Overview
The BliznOFF (Model/Catalog Number: BliznOFF) is a medical device manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification M9002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BliznOFF
- Product Code / EMDN
- M9002
- Device Name
- Scar Gel
- Database Sync Date
- 2026-08-09 16:47:32
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 BliznOFF?
The registered manufacturer of record for BliznOFF is LABORATOIRE L'IDEAL Parisien Sp. z o.o..
What is the Primary UDI-DI identifier for BliznOFF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903260909470.
What classification code is assigned to this device?
This device is registered under product classification code M9002.
Similar Classification Devices (M9002)
Other Devices by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
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