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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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NAD 1001000 — 1 UDI-DI variant, MDD (LEONARDINO SRL)

MD Atlas
LEONARDINO SRL

Data from EUDAMED, last updated May 31, 2026

NAD 1001000

B-08052870390318

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: LEONARDINO SRL

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: H60156678
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TUV Rheinland Italia SRL (1936)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-08052870390318
Device name: NAD 1001000
Device model: NAD 1001000
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Oct 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: LEONARDINO SRL
SRN: IT-MF-000029684
Country: Italy
Email: INFO@LEONARDINO.EU

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01K6YZCVCCFE34Z1JXBFDQZ803

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

NAD 100100008052870390318