eudamed_udi
Primary ID: 08053172970031
Fosfatasi Alcalina (DGKC) (UDI 08053172970031)
Manufactured by GIESSE DIAGNOSTICS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fosfatasi Alcalina (DGKC) - Primary ID 08053172970031
Device Regulatory Overview
The Fosfatasi Alcalina (DGKC) (Model/Catalog Number: 4096) is a medical device manufactured by GIESSE DIAGNOSTICS SRL. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4096
- Product Code / EMDN
- W01010105
- Device Name
- Fosfatasi Alcalina (DGKC)/Alkaline Phosphatase (DGCK)
- Database Sync Date
- 2026-08-09 16:47:19
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 Fosfatasi Alcalina (DGKC)?
The registered manufacturer of record for Fosfatasi Alcalina (DGKC) is GIESSE DIAGNOSTICS SRL.
What is the Primary UDI-DI identifier for Fosfatasi Alcalina (DGKC)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053172970031.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by GIESSE DIAGNOSTICS SRL
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