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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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K3 ENG FILE — 277 UDI-DI variants, MDR (KERR ITALIA SRL)

MD Atlas
KERR ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

K3 ENG FILE

80515118720000105C

277 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: KERR ITALIA SRL

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 80515118720000105C
Device name: K3 ENG FILE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: KERR ITALIA SRL
SRN: IT-MF-000007768
Country: Italy
Email: contact.kerritalia@envistaco.com

Variants by status

UDI-DI variants

277 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMJY7398QVN08W9GHR8BEFB3

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

QUANTEC ENG FILE08055165089058
QUANTEC ENG FILE08055165089454