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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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FLH-3 series — 4 UDI-DI variants, MDR (Ordisi, S.A)

MD Atlas
Ordisi, S.A

Data from EUDAMED, last updated May 23, 2026

FLH-3 series

84352050FLH3L6

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Ordisi, S.A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84352050FLH3L6
Device name: FLH-3 series
Device model: FLH311
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 25, 2021

Manufacturer & authorised representative

Manufacturer

Name: Ordisi, S.A
SRN: ES-MF-000000987
Country: Spain
Email: comercial@ordisi.com
Phone: +34 933 340 112

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FJKNDQQQM9R09FNRHZ0F9W9R

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

Examination lamp FLH-3 model w/rail holder, 35.000 lux08435205000043
FLH31108435205000012
Table mounted examination lamp FLH-3 model, 35.000 lux08435205000029
Wall mounted examination lamp FLH-3 model, 35.000 lux08435205000036