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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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RIGID ENDOSCOPE - LARYNGOSCOPE — 4 UDI-DI variants, MDR

MD Atlas
OPTOMIC ESPAÑA S.A

Data from EUDAMED, last updated May 30, 2026

RIGID ENDOSCOPE - LARYNGOSCOPE

84360415816423N

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: OPTOMIC ESPAÑA S.A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84360415816423N
Device name: RIGID ENDOSCOPE - LARYNGOSCOPE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: OPTOMIC ESPAÑA S.A
SRN: ES-MF-000003235
Country: Spain
Email: prrc@optomic.com
Phone: +34 91 804 44 44

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSJ8QRK0G4K7SVE223J1R5CW

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

3853365008436041580621
3853388008436041580669
3853388708436041580676
3853380308436041580638