KARAOĞLU (UDI 08699041010318)
Manufactured by KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ
Device Regulatory Overview
The KARAOĞLU (Model/Catalog Number: KD105.15) is a medical device manufactured by KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ. This product is indexed under FDA Product Code / Category Classification L031310 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KD105.15
- Product Code / EMDN
- L031310
- Device Name
- HOLDERS
- Database Sync Date
- 2026-08-09 16:28:47
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 KARAOĞLU?
The registered manufacturer of record for KARAOĞLU is KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ.
What is the Primary UDI-DI identifier for KARAOĞLU?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699041010318.
What classification code is assigned to this device?
This device is registered under product classification code L031310.
Similar Classification Devices (L031310)
Other Devices by KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ
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