eudamed_udi
Primary ID: 08033650840490
ALKALINE PHOSPHATASE FL DGKC (UDI 08033650840490)
Manufactured by Chema Diagnostica Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALKALINE PHOSPHATASE FL DGKC - Primary ID 08033650840490
Device Regulatory Overview
The ALKALINE PHOSPHATASE FL DGKC (Model/Catalog Number: AL F245 CH) is a medical device manufactured by Chema Diagnostica Srl. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AL F245 CH
- Product Code / EMDN
- W01010105
- Device Name
- ALKALINE PHOSPHATASE FL DGKC
- Database Sync Date
- 2026-08-09 16:51:13
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 ALKALINE PHOSPHATASE FL DGKC?
The registered manufacturer of record for ALKALINE PHOSPHATASE FL DGKC is Chema Diagnostica Srl.
What is the Primary UDI-DI identifier for ALKALINE PHOSPHATASE FL DGKC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033650840490.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by Chema Diagnostica Srl
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