eudamed_udi
Primary ID: 07640137453169
Bimanual I/A System reusable (T) (UDI 07640137453169)
Manufactured by Bürki inno med AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bimanual I/A System reusable (T) - Primary ID 07640137453169
Device Regulatory Overview
The Bimanual I/A System reusable (T) (Model/Catalog Number: BI 128/T) is a medical device manufactured by Bürki inno med AG. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BI 128/T
- Product Code / EMDN
- Q0299
- Device Name
- I/A System reusable
- Database Sync Date
- 2026-08-09 16:28:44
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 Bimanual I/A System reusable (T)?
The registered manufacturer of record for Bimanual I/A System reusable (T) is Bürki inno med AG.
What is the Primary UDI-DI identifier for Bimanual I/A System reusable (T)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640137453169.
What classification code is assigned to this device?
This device is registered under product classification code Q0299.
Similar Classification Devices (Q0299)
Other Devices by Bürki inno med AG
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