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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Lynx — 5 UDI-DI variants, MDR (PRISMA Srl)

MD Atlas
PRISMA Srl

Data from EUDAMED, last updated May 31, 2026

Lynx

805728949LYNXRJ

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: PRISMA Srl

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 805728949LYNXRJ
Device name: Lynx
Device model: LY-3.0-OR-RC-030-R
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: PRISMA Srl
SRN: IT-MF-000027140
Country: Italy
Email: info@prismaspine.com
Phone: +390792673216

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQ91ZKCBGQZNJW7W7921FTJK

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

LY-1.8-OR-RC-015-R08057289490048
LY-2.4-OR-RC-015-R08057289490024
LY-1.8-OR-RC-030-R08057289490031
LY-2.4-OR-RC-030-R08057289490017
LY-3.0-OR-RC-030-R08057289490000