gudid
Primary ID: WR090-01-0002
Colibr Primary Tube for VITEK 2 (UDI WR090-01-0002)
Manufactured by COPAN WASP SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Colibr Primary Tube for VITEK 2 - Primary ID WR090-01-0002
Device Regulatory Overview
The Colibr Primary Tube for VITEK 2 (Model/Catalog Number: WR090-01-0002) is a medical device manufactured by COPAN WASP SRL. This product is indexed under FDA Product Code / Category Classification LON within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WR090-01-0002
- Product Code / EMDN
- LON
- Device Name
- Colibr Primary Tube for VITEK 2
- Database Sync Date
- 2026-08-09 09:21:50
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 Colibr Primary Tube for VITEK 2?
The registered manufacturer of record for Colibr Primary Tube for VITEK 2 is COPAN WASP SRL.
What is the Primary UDI-DI identifier for Colibr Primary Tube for VITEK 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WR090-01-0002.
What classification code is assigned to this device?
This device is registered under product classification code LON.
Similar Classification Devices (LON)
Other Devices by COPAN WASP SRL
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