eudamed_udi
Primary ID: 00810026182617
Bipolar Forceps (UDI 00810026182617)
Manufactured by Soniquence, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bipolar Forceps - Primary ID 00810026182617
Device Regulatory Overview
The Bipolar Forceps (Model/Catalog Number: J19) is a medical device manufactured by Soniquence, LLC. This product is indexed under FDA Product Code / Category Classification L180401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- J19
- Product Code / EMDN
- L180401
- Device Name
- Bipolar Wand
- Database Sync Date
- 2026-08-09 16:44:49
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 Bipolar Forceps?
The registered manufacturer of record for Bipolar Forceps is Soniquence, LLC.
What is the Primary UDI-DI identifier for Bipolar Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810026182617.
What classification code is assigned to this device?
This device is registered under product classification code L180401.
Similar Classification Devices (L180401)
Other Devices by Soniquence, LLC
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