eudamed_udi
Primary ID: 06430080100248
Mueller-Hinton agar (MHA) herkkyysmalja (UDI 06430080100248)
Manufactured by Tammer BioLab Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mueller-Hinton agar (MHA) herkkyysmalja - Primary ID 06430080100248
Device Regulatory Overview
The Mueller-Hinton agar (MHA) herkkyysmalja (Model/Catalog Number: T070) is a medical device manufactured by Tammer BioLab Oy. This product is indexed under FDA Product Code / Category Classification W0104010403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T070
- Product Code / EMDN
- W0104010403
- Device Name
- Mueller-Hinton agar (MHA) herkkyysmalja
- Database Sync Date
- 2026-08-09 16:59:59
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 Mueller-Hinton agar (MHA) herkkyysmalja?
The registered manufacturer of record for Mueller-Hinton agar (MHA) herkkyysmalja is Tammer BioLab Oy.
What is the Primary UDI-DI identifier for Mueller-Hinton agar (MHA) herkkyysmalja?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100248.
What classification code is assigned to this device?
This device is registered under product classification code W0104010403.
Similar Classification Devices (W0104010403)
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