eudamed_udi
Primary ID: 06430080100262
Potato dextrose agarmalja [FI] (UDI 06430080100262)
Manufactured by Tammer BioLab Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Potato dextrose agarmalja [FI] - Primary ID 06430080100262
Device Regulatory Overview
The Potato dextrose agarmalja [FI] (Model/Catalog Number: T086) is a medical device manufactured by Tammer BioLab Oy. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T086
- Product Code / EMDN
- W0104030201
- Device Name
- Potato dextrose agarmalja
- Database Sync Date
- 2026-08-09 18:41:58
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 Potato dextrose agarmalja [FI]?
The registered manufacturer of record for Potato dextrose agarmalja [FI] is Tammer BioLab Oy.
What is the Primary UDI-DI identifier for Potato dextrose agarmalja [FI]?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100262.
What classification code is assigned to this device?
This device is registered under product classification code W0104030201.
Similar Classification Devices (W0104030201)
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