gudid
Primary ID: 242269
Artman Instruments (UDI 242269)
Manufactured by Wise Linkers, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Artman Instruments - Primary ID 242269
Device Regulatory Overview
The Artman Instruments (Model/Catalog Number: 242269) is a medical device manufactured by Wise Linkers, LLC. This product is indexed under FDA Product Code / Category Classification EKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 242269
- Product Code / EMDN
- EKB
- Device Name
- Dental Implant Depth Measuring Probe ARTMAN
- Database Sync Date
- 2026-08-09 09:01:55
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 Artman Instruments?
The registered manufacturer of record for Artman Instruments is Wise Linkers, LLC.
What is the Primary UDI-DI identifier for Artman Instruments?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 242269.
What classification code is assigned to this device?
This device is registered under product classification code EKB.
Similar Classification Devices (EKB)
Other Devices by Wise Linkers, LLC
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