eudamed_udi
Primary ID: 08699664030410
Dermapore (UDI 08699664030410)
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 Dermapore - Primary ID 08699664030410
Device Regulatory Overview
The Dermapore (Model/Catalog Number: S304) 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
- S304
- Product Code / EMDN
- M050199
- Device Name
- Surgical Tape
- Database Sync Date
- 2026-08-09 16:28:58
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Dermapore?
The registered manufacturer of record for Dermapore is SEYİTLER KİMYA SANAYİ A.Ş..
What is the Primary UDI-DI identifier for Dermapore?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699664030410.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint