GUDIDData
eudamed_udi Primary ID: 06430080100668

FAB rikasteliuos, 6 ml, painokorkki, iso putki (UDI 06430080100668)

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, painokorkki, iso putki - Primary ID 06430080100668

Device Regulatory Overview

The FAB rikasteliuos, 6 ml, painokorkki, iso putki (Model/Catalog Number: T038) 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
T038
Product Code / EMDN
W0104010206
Device Name
FAB rikasteliuos, 6 ml putki
Database Sync Date
2026-08-09 18:22:10

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of FAB rikasteliuos, 6 ml, painokorkki, iso putki?

The registered manufacturer of record for FAB rikasteliuos, 6 ml, painokorkki, iso putki is Tammer BioLab Oy.

What is the Primary UDI-DI identifier for FAB rikasteliuos, 6 ml, painokorkki, iso putki?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100668.

What classification code is assigned to this device?

This device is registered under product classification code W0104010206.

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