gudid
Primary ID: 000-A00650
Kirschner wire (1.2 x 80 mm) (UDI 000-A00650)
Manufactured by Keri Medical SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kirschner wire (1.2 x 80 mm) - Primary ID 000-A00650
Device Regulatory Overview
The Kirschner wire (1.2 x 80 mm) (Model/Catalog Number: 000-A00650) is a medical device manufactured by Keri Medical SA. This product is indexed under FDA Product Code / Category Classification HXI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 000-A00650
- Product Code / EMDN
- HXI
- Device Name
- Database Sync Date
- 2026-08-09 09:16:08
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 Kirschner wire (1.2 x 80 mm)?
The registered manufacturer of record for Kirschner wire (1.2 x 80 mm) is Keri Medical SA.
What is the Primary UDI-DI identifier for Kirschner wire (1.2 x 80 mm)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000-A00650.
What classification code is assigned to this device?
This device is registered under product classification code HXI.
Similar Classification Devices (HXI)
Other Devices by Keri Medical SA
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