Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

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

K3XF FILE08055165088587
K3XF FILE08055165088075
K3XF FILE08055165088778
K3XF FILE08055165088389
K3XF FILE08055165087870
K3XF FILE08055165088259
K3XF FILE08055165088334
K3XF FILE08055165088488
K3XF FILE08055165088518
K3XF FILE08055165088594
K3XF FILE08055165088235
K3XF FILE08055165088815
K3XF FILE08055165088952
K3XF FILE08055165087832
K3XF FILE08055165088884
K3XF FILE08055165088310
K3XF FILE08055165088136
K3XF FILE08055165088631
K3XF FILE08055165088532
K3XF FILE08055165088037
K3XF FILE08055165088358
K3XF FILE08055165088716
K3XF FILE08055165087924
K3XF FILE08055165088112
K3XF FILE08055165088792

4 5 6 7 8