eudamed_udi
Primary ID: 06944413815391
Test Cartridge (UDI 06944413815391)
Manufactured by Edan Instruments,Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Test Cartridge - Primary ID 06944413815391
Device Regulatory Overview
The Test Cartridge (Model/Catalog Number: iBG8) is a medical device manufactured by Edan Instruments,Inc.. This product is indexed under FDA Product Code / Category Classification W0101060605 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- iBG8
- Product Code / EMDN
- W0101060605
- Device Name
- Test Cartridge
- Database Sync Date
- 2026-08-09 16:44:53
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 Test Cartridge?
The registered manufacturer of record for Test Cartridge is Edan Instruments,Inc..
What is the Primary UDI-DI identifier for Test Cartridge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944413815391.
What classification code is assigned to this device?
This device is registered under product classification code W0101060605.
Similar Classification Devices (W0101060605)
Other Devices by Edan Instruments,Inc.
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