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.

QUADRO DI CENTRALE — 1 UDI-DI variant, MDD (D.Z. MEDICALE S.R.L.)

MD Atlas
D.Z. MEDICALE S.R.L.

Data from EUDAMED, last updated May 30, 2026

QUADRO DI CENTRALE

B-08059606105802

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: D.Z. MEDICALE S.R.L.

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

Active device

Legacy certificates

Certificate number: 0425-MED-003637-00
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ICIM S.P.A. (0425)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08059606105802
Device name: QUADRO DI CENTRALE
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: D.Z. MEDICALE S.R.L.
SRN: IT-MF-000013091
Country: Italy
Email: info@dzmedicalesrl.com
Phone: +390307268254

Variants by status

UDI-DI variants

1 UDI-DI variant

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

basicUdiUlid01KS9VQT4K0ZNX02JDTY27SEZ1

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

CENT26B08059606105802