eudamed_udi
Primary ID: 00841019106150
Aura (UDI 00841019106150)
Manufactured by Kirwan Surgical Products LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aura - Primary ID 00841019106150
Device Regulatory Overview
The Aura (Model/Catalog Number: 10-1403EAU) is a medical device manufactured by Kirwan Surgical Products LLC. This product is indexed under FDA Product Code / Category Classification L180401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-1403EAU
- Product Code / EMDN
- L180401
- Device Name
- Non-Stick Bipolar Coagulation Forceps 7 3/4 in. (19.7cm) Scoville-Greenwood Bayonet Insulated, 1.5mm tip
- Database Sync Date
- 2026-08-09 16:28:51
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 Aura?
The registered manufacturer of record for Aura is Kirwan Surgical Products LLC.
What is the Primary UDI-DI identifier for Aura?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841019106150.
What classification code is assigned to this device?
This device is registered under product classification code L180401.
Similar Classification Devices (L180401)
Other Devices by Kirwan Surgical Products LLC
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