eudamed_udi
Primary ID: 07073371017390
Aprikos (UDI 07073371017390)
Manufactured by Aprikos Medical AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aprikos - Primary ID 07073371017390
Device Regulatory Overview
The Aprikos (Model/Catalog Number: AM04-349-24) is a medical device manufactured by Aprikos Medical AS. This product is indexed under FDA Product Code / Category Classification L031306 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AM04-349-24
- Product Code / EMDN
- L031306
- Device Name
- LP-29 Hemostatic Forceps
- Database Sync Date
- 2026-08-09 16:28:55
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 Aprikos?
The registered manufacturer of record for Aprikos is Aprikos Medical AS.
What is the Primary UDI-DI identifier for Aprikos?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07073371017390.
What classification code is assigned to this device?
This device is registered under product classification code L031306.
Similar Classification Devices (L031306)
Other Devices by Aprikos Medical AS
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