Karsel (UDI 08681198503195)
Manufactured by Kardeşler Tıbbi Cihazlar Ticaret Limited Şirket
Device Regulatory Overview
The Karsel (Model/Catalog Number: KSFR215200) is a medical device manufactured by Kardeşler Tıbbi Cihazlar Ticaret Limited Şirket. This product is indexed under FDA Product Code / Category Classification S01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KSFR215200
- Product Code / EMDN
- S01020101
- Device Name
- Sterilization Products
- Database Sync Date
- 2026-08-09 16:46:29
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 Karsel?
The registered manufacturer of record for Karsel is Kardeşler Tıbbi Cihazlar Ticaret Limited Şirket.
What is the Primary UDI-DI identifier for Karsel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681198503195.
What classification code is assigned to this device?
This device is registered under product classification code S01020101.
Similar Classification Devices (S01020101)
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