eudamed_udi
Primary ID: 05056863357862
WELDON INSTRUMENTS (UDI 05056863357862)
Manufactured by Weldon Instruments
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WELDON INSTRUMENTS - Primary ID 05056863357862
Device Regulatory Overview
The WELDON INSTRUMENTS (Model/Catalog Number: WD-145-002-HHR) is a medical device manufactured by Weldon Instruments. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WD-145-002-HHR
- Product Code / EMDN
- L159003
- Device Name
- WD-145-002-HHR: Non-Sterile, Reusable, Dental Explorer, Fig. 9
- Database Sync Date
- 2026-08-09 16:28:46
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 WELDON INSTRUMENTS?
The registered manufacturer of record for WELDON INSTRUMENTS is Weldon Instruments.
What is the Primary UDI-DI identifier for WELDON INSTRUMENTS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056863357862.
What classification code is assigned to this device?
This device is registered under product classification code L159003.
Similar Classification Devices (L159003)
Other Devices by Weldon Instruments
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