eudamed_udi
Primary ID: 08054187139215
DESOXYCHOLATE AGAR - 500 g (UDI 08054187139215)
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 DESOXYCHOLATE AGAR - 500 g - Primary ID 08054187139215
Device Regulatory Overview
The DESOXYCHOLATE AGAR - 500 g (Model/Catalog Number: 4013702) 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
- 4013702
- Product Code / EMDN
- W0104010101
- Device Name
- COLUMBIA AGAR BASE - 500 g
- Database Sync Date
- 2026-08-09 16:30:26
Full Regulatory Attributes
🔒 Token Gated
{
"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 DESOXYCHOLATE AGAR - 500 g?
The registered manufacturer of record for DESOXYCHOLATE AGAR - 500 g is Biolife Italiana s.r.l..
What is the Primary UDI-DI identifier for DESOXYCHOLATE AGAR - 500 g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054187139215.
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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