eudamed_udi
Primary ID: 05940540383438
AGAR SOIA TRIPTIC (SANGE CAL 5%) (UDI 05940540383438)
Manufactured by DELTAROM SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AGAR SOIA TRIPTIC (SANGE CAL 5%) - Primary ID 05940540383438
Device Regulatory Overview
The AGAR SOIA TRIPTIC (SANGE CAL 5%) (Model/Catalog Number: 341365) is a medical device manufactured by DELTAROM SRL. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 341365
- Product Code / EMDN
- W0104010101
- Device Name
- AGAR SOIA TRIPTIC (SANGE CAL 5%)
- Database Sync Date
- 2026-08-09 16:29:22
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 AGAR SOIA TRIPTIC (SANGE CAL 5%)?
The registered manufacturer of record for AGAR SOIA TRIPTIC (SANGE CAL 5%) is DELTAROM SRL.
What is the Primary UDI-DI identifier for AGAR SOIA TRIPTIC (SANGE CAL 5%)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540383438.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by DELTAROM SRL
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