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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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SPECULUM MONOUSO STERILE CHIUSURA A VITE — 6 UDI-DI variants, MDR

MD Atlas
Kaltek S.r.l.

Data from EUDAMED, last updated May 30, 2026

SPECULUM MONOUSO STERILE CHIUSURA A VITE

805551056speculum_ster45

6 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: Kaltek S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805551056speculum_ster45
Device name: SPECULUM MONOUSO STERILE CHIUSURA A VITE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Kaltek S.r.l.
SRN: IT-MF-000019573
Country: Italy
Email: info@kaltek.it
Phone: +39 0498703410

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMD5S28HG1GA8KFXVJRS7H6H

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

081408055510561000
081308055510560997
229508055510561017
080108055510560980
080308055510560973
080008055510560966