eudamed_udi
Primary ID: 05032384575022
TRYPTONE SOYA BROTH EP/USP/BP/JP (UDI 05032384575022)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRYPTONE SOYA BROTH EP/USP/BP/JP - Primary ID 05032384575022
Device Regulatory Overview
The TRYPTONE SOYA BROTH EP/USP/BP/JP (Model/Catalog Number: CM0129AU) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CM0129AU
- Product Code / EMDN
- W0104010101
- Device Name
- TRYPTONE SOYA BROTH
- Database Sync Date
- 2026-08-09 16:48:46
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 TRYPTONE SOYA BROTH EP/USP/BP/JP?
The registered manufacturer of record for TRYPTONE SOYA BROTH EP/USP/BP/JP is Oxoid Ltd.
What is the Primary UDI-DI identifier for TRYPTONE SOYA BROTH EP/USP/BP/JP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384575022.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
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