eudamed_udi
Primary ID: 08053172970123
ALT/GPT (UDI 08053172970123)
Manufactured by GIESSE DIAGNOSTICS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALT/GPT - Primary ID 08053172970123
Device Regulatory Overview
The ALT/GPT (Model/Catalog Number: 4194) is a medical device manufactured by GIESSE DIAGNOSTICS SRL. This product is indexed under FDA Product Code / Category Classification W01010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4194
- Product Code / EMDN
- W01010103
- Device Name
- ALT/GPT
- Database Sync Date
- 2026-08-09 16:29:50
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 ALT/GPT?
The registered manufacturer of record for ALT/GPT is GIESSE DIAGNOSTICS SRL.
What is the Primary UDI-DI identifier for ALT/GPT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053172970123.
What classification code is assigned to this device?
This device is registered under product classification code W01010103.
Similar Classification Devices (W01010103)
Other Devices by GIESSE DIAGNOSTICS SRL
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