gudid
Primary ID: 0240-099-265
Stryker (UDI 0240-099-265)
Manufactured by Barco, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Stryker - Primary ID 0240-099-265
Device Regulatory Overview
The Stryker (Model/Catalog Number: 0240-099-265) is a medical device manufactured by Barco, Inc.. This product is indexed under FDA Product Code / Category Classification FWB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0240-099-265
- Product Code / EMDN
- FWB
- Device Name
- DVI to HDMI Converter
- Database Sync Date
- 2026-08-09 09:04:15
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 Stryker?
The registered manufacturer of record for Stryker is Barco, Inc..
What is the Primary UDI-DI identifier for Stryker?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0240-099-265.
What classification code is assigned to this device?
This device is registered under product classification code FWB.
Similar Classification Devices (FWB)
Other Devices by Barco, Inc.
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