CANSINFİX TIBBİ ESNEK FLASTER (UDI 08699721130763)
Manufactured by CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ
Device Regulatory Overview
The CANSINFİX TIBBİ ESNEK FLASTER (Model/Catalog Number: 65) is a medical device manufactured by CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 65
- Product Code / EMDN
- M050101
- Device Name
- CANSINPLAST HİPOALERJİK FLASTER
- Database Sync Date
- 2026-08-09 16:44:52
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 CANSINFİX TIBBİ ESNEK FLASTER?
The registered manufacturer of record for CANSINFİX TIBBİ ESNEK FLASTER is CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for CANSINFİX TIBBİ ESNEK FLASTER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699721130763.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ
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