eudamed_udi
Primary ID: 08800042702694
ArtiSential Graspers (UDI 08800042702694)
Manufactured by LivsMed Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ArtiSential Graspers - Primary ID 08800042702694
Device Regulatory Overview
The ArtiSential Graspers (Model/Catalog Number: 5AUF01-LV) is a medical device manufactured by LivsMed Inc.. This product is indexed under FDA Product Code / Category Classification K01020104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5AUF01-LV
- Product Code / EMDN
- K01020104
- Device Name
- Laparoscopic Instruments - Graspers
- Database Sync Date
- 2026-08-09 16:46:55
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 ArtiSential Graspers?
The registered manufacturer of record for ArtiSential Graspers is LivsMed Inc..
What is the Primary UDI-DI identifier for ArtiSential Graspers?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800042702694.
What classification code is assigned to this device?
This device is registered under product classification code K01020104.
Similar Classification Devices (K01020104)
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