eudamed_udi
Primary ID: 03573026048440
API® 20 STREP (UDI 03573026048440)
Manufactured by bioMérieux SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for API® 20 STREP - Primary ID 03573026048440
Device Regulatory Overview
The API® 20 STREP (Model/Catalog Number: 20600) is a medical device manufactured by bioMérieux SA. This product is indexed under FDA Product Code / Category Classification W0104080203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20600
- Product Code / EMDN
- W0104080203
- Device Name
- API® 20 STREP
- Database Sync Date
- 2026-08-09 18:32:27
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 API® 20 STREP?
The registered manufacturer of record for API® 20 STREP is bioMérieux SA.
What is the Primary UDI-DI identifier for API® 20 STREP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03573026048440.
What classification code is assigned to this device?
This device is registered under product classification code W0104080203.
Similar Classification Devices (W0104080203)
Other Devices by bioMérieux SA
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