eudamed_udi
Primary ID: 03532679226605
STREPTATEST (UDI 03532679226605)
Manufactured by BIOSYNEX
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STREPTATEST - Primary ID 03532679226605
Device Regulatory Overview
The STREPTATEST (Model/Catalog Number: 10025) is a medical device manufactured by BIOSYNEX. This product is indexed under FDA Product Code / Category Classification W0105011101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10025
- Product Code / EMDN
- W0105011101
- Device Name
- STREPTATEST
- Database Sync Date
- 2026-08-09 16:28:52
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 STREPTATEST?
The registered manufacturer of record for STREPTATEST is BIOSYNEX.
What is the Primary UDI-DI identifier for STREPTATEST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03532679226605.
What classification code is assigned to this device?
This device is registered under product classification code W0105011101.
Similar Classification Devices (W0105011101)
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