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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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KAMILLA — 3 UDI-DI variants, MDR (MORFEUS S.p.A.)

MD Atlas
MORFEUS S.p.A.

Data from EUDAMED, last updated May 31, 2026

KAMILLA

8028540M7034KX

3 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: MORFEUS S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8028540M7034KX
Device name: KAMILLA
Device model: KAMILLA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: MORFEUS S.p.A.
SRN: IT-MF-000046753
Country: Italy
Email: morfeus@morfeus.it
Phone: +390722629611

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS7BAH8SNVQCDKF6HSG20BZ9

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

703408028540002560
703408028540002577
703408028540002553