eudamed_udi
Primary ID: 08426950589457
BIO-FLASH Screw Caps for Sample Cups (UDI 08426950589457)
Manufactured by Biokit S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIO-FLASH Screw Caps for Sample Cups - Primary ID 08426950589457
Device Regulatory Overview
The BIO-FLASH Screw Caps for Sample Cups (Model/Catalog Number: 3000-8210) is a medical device manufactured by Biokit S.A.. This product is indexed under FDA Product Code / Category Classification W0201020185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3000-8210
- Product Code / EMDN
- W0201020185
- Device Name
- BIO-FLASH
- Database Sync Date
- 2026-08-09 16:49:00
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 BIO-FLASH Screw Caps for Sample Cups?
The registered manufacturer of record for BIO-FLASH Screw Caps for Sample Cups is Biokit S.A..
What is the Primary UDI-DI identifier for BIO-FLASH Screw Caps for Sample Cups?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08426950589457.
What classification code is assigned to this device?
This device is registered under product classification code W0201020185.
Similar Classification Devices (W0201020185)
Other Devices by Biokit S.A.
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