gudid
Primary ID: W090
Colibr (UDI W090)
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 ID W090
Device Regulatory Overview
The Colibr (Model/Catalog Number: W090) 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
- W090
- Product Code / EMDN
- LON
- Device Name
- Colibr
- Database Sync Date
- 2026-08-09 09:16:47
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?
The registered manufacturer of record for Colibr is COPAN WASP SRL.
What is the Primary UDI-DI identifier for Colibr?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W090.
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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