Alisklamp Klasik (UDI 08699255010104)
Manufactured by ABA GRUP SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The Alisklamp Klasik (Model/Catalog Number: AK-26) is a medical device manufactured by ABA GRUP SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification K01020104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AK-26
- Product Code / EMDN
- K01020104
- Device Name
- DISPOSABLE CIRCUMCISION CLAMP NO:10
- Database Sync Date
- 2026-08-09 16:44:50
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 Alisklamp Klasik?
The registered manufacturer of record for Alisklamp Klasik is ABA GRUP SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for Alisklamp Klasik?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699255010104.
What classification code is assigned to this device?
This device is registered under product classification code K01020104.
Similar Classification Devices (K01020104)
Other Devices by ABA GRUP SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ
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