eudamed_udi
Primary ID: 07640137451844
Monomanual I/A System reusable (UDI 07640137451844)
Manufactured by Bürki inno med AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Monomanual I/A System reusable - Primary ID 07640137451844
Device Regulatory Overview
The Monomanual I/A System reusable (Model/Catalog Number: SL 118 c2) 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
- SL 118 c2
- Product Code / EMDN
- Q0299
- Device Name
- I/A System reusable
- Database Sync Date
- 2026-08-09 18:25:14
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 Monomanual I/A System reusable?
The registered manufacturer of record for Monomanual I/A System reusable is Bürki inno med AG.
What is the Primary UDI-DI identifier for Monomanual I/A System reusable?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640137451844.
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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