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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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19G VISCOUS FLUID REMOVAL KIT — 4 UDI-DI variants, MDR

MD Atlas
Optikon 2000 S.p.A.

Data from EUDAMED, last updated May 30, 2026

19G VISCOUS FLUID REMOVAL KIT

8059308SUR_INF_016UC

4 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: Optikon 2000 S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8059308SUR_INF_016UC
Device name: 19G VISCOUS FLUID REMOVAL KIT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Optikon 2000 S.p.A.
SRN: IT-MF-000017618
Country: Italy
Email: mronchetti@bvimedical.com
Phone: +39 06 8888410

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KQA4D0P1CZF289K9NA89YPSJ

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

192525 08059308002621
19270308059308010411
19255008059308009590
19254008059308009583