eudamed_udi
Primary ID: 04251143403531
4-motion® Tibia-Größenlehre Gr. 9 (UDI 04251143403531)
Manufactured by ARTIQO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 4-motion® Tibia-Größenlehre Gr. 9 - Primary ID 04251143403531
Device Regulatory Overview
The 4-motion® Tibia-Größenlehre Gr. 9 (Model/Catalog Number: 9210909) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification L091199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9210909
- Product Code / EMDN
- L091199
- Device Name
- Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; Probeimplantate
- Database Sync Date
- 2026-08-09 16:46:26
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 4-motion® Tibia-Größenlehre Gr. 9?
The registered manufacturer of record for 4-motion® Tibia-Größenlehre Gr. 9 is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® Tibia-Größenlehre Gr. 9?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143403531.
What classification code is assigned to this device?
This device is registered under product classification code L091199.
Similar Classification Devices (L091199)
Other Devices by ARTIQO GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint