ΑΛΚ.ΦΩΣΦΑΤΑΣΗ DGKC R1:4x36, R2:2x18 ml (GSAU) (UDI 05213003193630)
Manufactured by Biotechnological Applications Ltd
Device Regulatory Overview
The ΑΛΚ.ΦΩΣΦΑΤΑΣΗ DGKC R1:4x36, R2:2x18 ml (GSAU) (Model/Catalog Number: 002210) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002210
- Product Code / EMDN
- W01010105
- Device Name
- ΑΛΚ.ΦΩΣΦΑΤΑΣΗ DGKC R1:4x36, R2:2x18 ml (GSAU)
- Database Sync Date
- 2026-08-09 16:29:54
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 ΑΛΚ.ΦΩΣΦΑΤΑΣΗ DGKC R1:4x36, R2:2x18 ml (GSAU)?
The registered manufacturer of record for ΑΛΚ.ΦΩΣΦΑΤΑΣΗ DGKC R1:4x36, R2:2x18 ml (GSAU) is Biotechnological Applications Ltd.
What is the Primary UDI-DI identifier for ΑΛΚ.ΦΩΣΦΑΤΑΣΗ DGKC R1:4x36, R2:2x18 ml (GSAU)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003193630.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by Biotechnological Applications Ltd
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