eudamed_udi
Primary ID: 00887761982222
Liko (UDI 00887761982222)
Manufactured by Liko Aktiebolag
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Liko - Primary ID 00887761982222
Device Regulatory Overview
The Liko (Model/Catalog Number: 3126036) is a medical device manufactured by Liko Aktiebolag. This product is indexed under FDA Product Code / Category Classification V08050302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3126036
- Product Code / EMDN
- V08050302
- Device Name
- Overhead Lift, battery-powered
- Database Sync Date
- 2026-08-09 16:28:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Liko?
The registered manufacturer of record for Liko is Liko Aktiebolag.
What is the Primary UDI-DI identifier for Liko?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00887761982222.
What classification code is assigned to this device?
This device is registered under product classification code V08050302.
Similar Classification Devices (V08050302)
Other Devices by Liko Aktiebolag
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint