eudamed_udi
Primary ID: 08699664020312
Dermafix Plus (UDI 08699664020312)
Manufactured by SEYİTLER KİMYA SANAYİ A.Ş.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dermafix Plus - Primary ID 08699664020312
Device Regulatory Overview
The Dermafix Plus (Model/Catalog Number: S203) is a medical device manufactured by SEYİTLER KİMYA SANAYİ A.Ş.. This product is indexed under FDA Product Code / Category Classification M050199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S203
- Product Code / EMDN
- M050199
- Device Name
- Surgical Tape
- Database Sync Date
- 2026-08-09 17:17:31
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 Dermafix Plus?
The registered manufacturer of record for Dermafix Plus is SEYİTLER KİMYA SANAYİ A.Ş..
What is the Primary UDI-DI identifier for Dermafix Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699664020312.
What classification code is assigned to this device?
This device is registered under product classification code M050199.
Similar Classification Devices (M050199)
Other Devices by SEYİTLER KİMYA SANAYİ A.Ş.
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