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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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L2-9 — 2 UDI-DI variants, MDR (Parallel Design SAS)

MD Atlas
Parallel Design SAS

Data from EUDAMED, last updated May 19, 2026

L2-9

8406821BUG00335HE

2 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: Parallel Design SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8406821BUG00335HE
Device name: L2-9
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 20, 2024

Manufacturer & authorised representative

Manufacturer

Name: Parallel Design SAS
SRN: FR-MF-000001806
Country: France
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H7AM12QWKZ54WJGJQPHFYV68

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

574528000840682124355
575480600840682124768