Unspecified Brand (UDI 08698712455274)
Manufactured by TURKUAZ SAĞLIK HİZMETLERİ MEDİKAL TEMİZLİK KİMYASAL ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: AFS-0001) is a medical device manufactured by TURKUAZ SAĞLIK HİZMETLERİ MEDİKAL TEMİZLİK KİMYASAL ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification U0803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AFS-0001
- Product Code / EMDN
- U0803
- Device Name
- KONIX LAPAROSCOPIC LENS ANTI-FOG SOLUTION AND SPONGE 6 ML
- Database Sync Date
- 2026-08-09 16:47:58
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is TURKUAZ SAĞLIK HİZMETLERİ MEDİKAL TEMİZLİK KİMYASAL ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698712455274.
What classification code is assigned to this device?
This device is registered under product classification code U0803.
Similar Classification Devices (U0803)
Other Devices by TURKUAZ SAĞLIK HİZMETLERİ MEDİKAL TEMİZLİK KİMYASAL ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ
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