gudid
Primary ID: TEST1 2.0
TEST1 2.0 (UDI TEST1 2.0)
Manufactured by ALIFAX SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TEST1 2.0 - Primary ID TEST1 2.0
Device Regulatory Overview
The TEST1 2.0 (Model/Catalog Number: TEST1 2.0) 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 2.0
- Product Code / EMDN
- GKB
- Device Name
- 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 2.0?
The registered manufacturer of record for TEST1 2.0 is ALIFAX SRL.
What is the Primary UDI-DI identifier for TEST1 2.0?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TEST1 2.0.
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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