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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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Twister — 36 UDI-DI variants, MDR (Ceram Optec SIA)

MD Atlas
Ceram Optec SIA

Data from EUDAMED, last updated May 31, 2026

Twister

404908904NT

36 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: Ceram Optec SIA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 404908904NT
Device name: Twister
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ceram Optec SIA
SRN: LV-MF-000021846
Country: Latvia
Email: infolv@ceramoptec.com
Phone: +371 653 43 646

Variants by status

UDI-DI variants

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRKH107VXSJMR9XK2HA6PK4A

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

50180222004049089005403
50320077704049089005601
50110041004049089005700
50520090004049089005687
50180522004049089005427
50320076004049089005564
50320025004049089005342
50320022004049089005458
50120025004049089005335
50130045004049089005304
50320032904049089005724

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