eudamed_udi
Primary ID: 08033650840544
ALKALINE PHOSPHATASE FL IFCC (UDI 08033650840544)
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 IFCC - Primary ID 08033650840544
Device Regulatory Overview
The ALKALINE PHOSPHATASE FL IFCC (Model/Catalog Number: AF F400 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
- AF F400 CH
- Product Code / EMDN
- W01010105
- Device Name
- ALKALINE PHOSPHATASE FL IFCC
- Database Sync Date
- 2026-08-09 17:10:09
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 IFCC?
The registered manufacturer of record for ALKALINE PHOSPHATASE FL IFCC is Chema Diagnostica Srl.
What is the Primary UDI-DI identifier for ALKALINE PHOSPHATASE FL IFCC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033650840544.
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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