ONECARE (UDI 08682560953303)
Manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The ONECARE (Model/Catalog Number: D1) is a medical device manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification Q01010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D1
- Product Code / EMDN
- Q01010299
- Device Name
- SODIUM HYPOCHLORITE 5%
- Database Sync Date
- 2026-08-09 16:58:25
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 ONECARE?
The registered manufacturer of record for ONECARE is KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for ONECARE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682560953303.
What classification code is assigned to this device?
This device is registered under product classification code Q01010299.
Similar Classification Devices (Q01010299)
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