eudamed_udi
Primary ID: 08683020071865
EEG PASTE (UDI 08683020071865)
Manufactured by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EEG PASTE - Primary ID 08683020071865
Device Regulatory Overview
The EEG PASTE (Model/Catalog Number: ALG-EEG13) is a medical device manufactured by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Z12100385 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALG-EEG13
- Product Code / EMDN
- Z12100385
- Device Name
- EEG PASTE
- Database Sync Date
- 2026-08-09 16:58:47
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 EEG PASTE?
The registered manufacturer of record for EEG PASTE is ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ..
What is the Primary UDI-DI identifier for EEG PASTE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683020071865.
What classification code is assigned to this device?
This device is registered under product classification code Z12100385.
Similar Classification Devices (Z12100385)
Other Devices by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.
Programmatic Export
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