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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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Precisio — 1 UDI-DI variant, MDD (iVis Technologies S.r.l.)

MD Atlas
iVis Technologies S.r.l.

Data from EUDAMED, last updated May 30, 2026

Precisio

B-PX001YN

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: iVis Technologies S.r.l.

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: G10871850004
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: May 25, 2024

Identity & classification

Basic UDI-DI: B-PX001YN
Device name: Precisio
Device model: PX001
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Nov 29, 2021

Manufacturer & authorised representative

Manufacturer

Name: iVis Technologies S.r.l.
SRN: IT-MF-000016859
Country: Italy
Email: g.dippolito@ivistechnologies.com
Phone: +390997791680

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FNNZJZ65Y7RKKAWPA1MD2CZS

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

PrecisioD-PX001YN