eudamed_udi
Primary ID: 08054187133732
TRYPTIC SOY BROTH - 5 Kg (UDI 08054187133732)
Manufactured by Biolife Italiana s.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRYPTIC SOY BROTH - 5 Kg - Primary ID 08054187133732
Device Regulatory Overview
The TRYPTIC SOY BROTH - 5 Kg (Model/Catalog Number: 4021554) is a medical device manufactured by Biolife Italiana s.r.l.. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4021554
- Product Code / EMDN
- W0104010101
- Device Name
- COLUMBIA AGAR BASE - 500 g
- Database Sync Date
- 2026-08-09 16:29:18
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 TRYPTIC SOY BROTH - 5 Kg?
The registered manufacturer of record for TRYPTIC SOY BROTH - 5 Kg is Biolife Italiana s.r.l..
What is the Primary UDI-DI identifier for TRYPTIC SOY BROTH - 5 Kg?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054187133732.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by Biolife Italiana s.r.l.
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