Kösemed (UDI D-86820355026926N)
Manufactured by KÖSEMED ORTOPEDİ SAN. VE TİC. İTH. İHR. A.Ş.
Device Regulatory Overview
The Kösemed (Model/Catalog Number: 522-03) is a medical device manufactured by KÖSEMED ORTOPEDİ SAN. VE TİC. İTH. İHR. A.Ş.. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 522-03
- Product Code / EMDN
- Y060603
- Device Name
- KURBAĞA PARMAK ATELİ NO:3
- Database Sync Date
- 2026-08-09 16:28:51
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 Kösemed?
The registered manufacturer of record for Kösemed is KÖSEMED ORTOPEDİ SAN. VE TİC. İTH. İHR. A.Ş..
What is the Primary UDI-DI identifier for Kösemed?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-86820355026926N.
What classification code is assigned to this device?
This device is registered under product classification code Y060603.
Similar Classification Devices (Y060603)
Other Devices by KÖSEMED ORTOPEDİ SAN. VE TİC. İTH. İHR. A.Ş.
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