eudamed_udi
Primary ID: 03532670100348
DRUGCHECK+ OXY (UDI 03532670100348)
Manufactured by BIOSYNEX Swiss SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DRUGCHECK+ OXY - Primary ID 03532670100348
Device Regulatory Overview
The DRUGCHECK+ OXY (Model/Catalog Number: 1140023_SW) is a medical device manufactured by BIOSYNEX Swiss SA. This product is indexed under FDA Product Code / Category Classification W0102160508 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1140023_SW
- Product Code / EMDN
- W0102160508
- Device Name
- DRUGCHECK+ OXY
- Database Sync Date
- 2026-08-09 16:30:32
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 DRUGCHECK+ OXY?
The registered manufacturer of record for DRUGCHECK+ OXY is BIOSYNEX Swiss SA.
What is the Primary UDI-DI identifier for DRUGCHECK+ OXY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03532670100348.
What classification code is assigned to this device?
This device is registered under product classification code W0102160508.
Similar Classification Devices (W0102160508)
Other Devices by BIOSYNEX Swiss SA
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