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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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CONTENITORE PRECARICATO CON… — 12 UDI-DI variants, IVDR

MD Atlas
Kaltek S.r.l.

Data from EUDAMED, last updated May 30, 2026

CONTENITORE PRECARICATO CON FORMALDEIDE 4%

805551056cont_precarAT

12 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Kaltek S.r.l.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 805551056cont_precarAT
Device name: CONTENITORE PRECARICATO CON FORMALDEIDE 4%
Device model: CONTENITORE PRECARICATO CON FORMALDEIDE 4%
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 2, 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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KN7J1KHMHZHS2N7QDYEKQPCE

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

159208055510563103
159608055510563141
158608055510563189
159308055510563110
159708055510563158
159408055510563127
159108055510563097
159808055510563165
159508055510563134
159908055510563172
158908055510563080
159008055510563073