eudamed_udi
Primary ID: 06430080100125
FAB rikasteliuos, 6 ml putki (UDI 06430080100125)
Manufactured by Tammer BioLab Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FAB rikasteliuos, 6 ml putki - Primary ID 06430080100125
Device Regulatory Overview
The FAB rikasteliuos, 6 ml putki (Model/Catalog Number: T037) is a medical device manufactured by Tammer BioLab Oy. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T037
- Product Code / EMDN
- W0104010206
- Device Name
- FAB rikasteliuos, 6 ml putki
- Database Sync Date
- 2026-08-09 18:41:45
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 FAB rikasteliuos, 6 ml putki?
The registered manufacturer of record for FAB rikasteliuos, 6 ml putki is Tammer BioLab Oy.
What is the Primary UDI-DI identifier for FAB rikasteliuos, 6 ml putki?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100125.
What classification code is assigned to this device?
This device is registered under product classification code W0104010206.
Similar Classification Devices (W0104010206)
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