eudamed_udi
Primary ID: 08683020073418
DERMOSEPT MULTI-AS (UDI 08683020073418)
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 DERMOSEPT MULTI-AS - Primary ID 08683020073418
Device Regulatory Overview
The DERMOSEPT MULTI-AS (Model/Catalog Number: ALG24-07) is a medical device manufactured by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification D0899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALG24-07
- Product Code / EMDN
- D0899
- Device Name
- DERMOSEPT MULTI-AS CONCENTRATED MEDICAL INSTRUMENT CLEANING AND MAINTENANCE SOLUTION – PHOSPHORIC ACID
- Database Sync Date
- 2026-08-09 16:46:14
Full Regulatory Attributes
🔒 Token Gated
{
"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 DERMOSEPT MULTI-AS?
The registered manufacturer of record for DERMOSEPT MULTI-AS is ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ..
What is the Primary UDI-DI identifier for DERMOSEPT MULTI-AS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683020073418.
What classification code is assigned to this device?
This device is registered under product classification code D0899.
Similar Classification Devices (D0899)
Other Devices by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.
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