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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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UNIKO PZ — 9 UDI-DI variants, MDR (MARIOTTI & C. S.R.L.)

MD Atlas
MARIOTTI & C. S.R.L.

Data from EUDAMED, last updated May 31, 2026

UNIKO PZ

805674633SURDEVTL

9 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: MARIOTTI & C. S.R.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805674633SURDEVTL
Device name: UNIKO PZ
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: MARIOTTI & C. S.R.L.
SRN: IT-MF-000035061
Country: Italy
Email: info@mariotti-italy.com
Phone: +39 0543 781811

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGHCETEPVADKMTP50TJTX3H0

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

UNIKO PZ08056746330002
MiniUNIKO C08056746330026
MiniUNIKO PZ08056746330040
MiniUNIKO PZL08056746330309
PHYSIO-F308056746330392
MiniUNIKO G08056746330323
PRAD-208056746330385
MiniUNIKO F08056746330033
MiniUNIKO C.L08056746330019