eudamed_udi
Primary ID: 05032384002757
GC AGAR BASE (UDI 05032384002757)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GC AGAR BASE - Primary ID 05032384002757
Device Regulatory Overview
The GC AGAR BASE (Model/Catalog Number: CM0367K) 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
- CM0367K
- Product Code / EMDN
- W0104010101
- Device Name
- GC AGAR
- Database Sync Date
- 2026-08-09 16:30:11
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 GC AGAR BASE?
The registered manufacturer of record for GC AGAR BASE is Oxoid Ltd.
What is the Primary UDI-DI identifier for GC AGAR BASE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384002757.
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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