gudid
Primary ID: TEST1 THL
TEST1 THL (UDI TEST1 THL)
Manufactured by ALIFAX SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TEST1 THL - Primary ID TEST1 THL
Device Regulatory Overview
The TEST1 THL (Model/Catalog Number: TEST1 THL) is a medical device manufactured by ALIFAX SRL. This product is indexed under FDA Product Code / Category Classification GKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TEST1 THL
- Product Code / EMDN
- GKB
- Device Name
- TEST-1 THL - ESR automated analyzer, with Software for Latex Controls. Using different CBC rack metal adaptors.
- Database Sync Date
- 2026-08-09 09:04:30
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 TEST1 THL?
The registered manufacturer of record for TEST1 THL is ALIFAX SRL.
What is the Primary UDI-DI identifier for TEST1 THL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TEST1 THL.
What classification code is assigned to this device?
This device is registered under product classification code GKB.
Similar Classification Devices (GKB)
Other Devices by ALIFAX SRL
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