eudamed_udi
Primary ID: 05032384020652
SAB DEX AGAR + CHLORAMPHENICOL SLOPE (UDI 05032384020652)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SAB DEX AGAR + CHLORAMPHENICOL SLOPE - Primary ID 05032384020652
Device Regulatory Overview
The SAB DEX AGAR + CHLORAMPHENICOL SLOPE (Model/Catalog Number: BO0422F) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104030303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BO0422F
- Product Code / EMDN
- W0104030303
- Device Name
- SAB DEX AGAR + CHLORAMPHENICOL SLOPE
- Database Sync Date
- 2026-08-09 16:46:47
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 SAB DEX AGAR + CHLORAMPHENICOL SLOPE?
The registered manufacturer of record for SAB DEX AGAR + CHLORAMPHENICOL SLOPE is Oxoid Ltd.
What is the Primary UDI-DI identifier for SAB DEX AGAR + CHLORAMPHENICOL SLOPE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384020652.
What classification code is assigned to this device?
This device is registered under product classification code W0104030303.
Similar Classification Devices (W0104030303)
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