eudamed_udi
Primary ID: 06430080100361
Soija-kaseiiniliuos, 4 ml putki [FI] (UDI 06430080100361)
Manufactured by Tammer BioLab Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Soija-kaseiiniliuos, 4 ml putki [FI] - Primary ID 06430080100361
Device Regulatory Overview
The Soija-kaseiiniliuos, 4 ml putki [FI] (Model/Catalog Number: T128) 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
- T128
- Product Code / EMDN
- W0104010206
- Device Name
- Soija-kaseiiniliuos, 4 ml putki
- Database Sync Date
- 2026-08-09 17:38:49
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 Soija-kaseiiniliuos, 4 ml putki [FI]?
The registered manufacturer of record for Soija-kaseiiniliuos, 4 ml putki [FI] is Tammer BioLab Oy.
What is the Primary UDI-DI identifier for Soija-kaseiiniliuos, 4 ml putki [FI]?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100361.
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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