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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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MICRONEBULIZZATORE — 6 UDI-DI variants, MDR (Amil Care Italia S.r.l.)

MD Atlas
Amil Care Italia S.r.l.

Data from EUDAMED, last updated May 30, 2026

MICRONEBULIZZATORE

805664647TB21tFV

6 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: Amil Care Italia S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805664647TB21tFV
Device name: MICRONEBULIZZATORE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Amil Care Italia S.r.l.
SRN: IT-MF-000012107
Country: Italy
Email: capobianco@amilcareitalia.com
Phone: +39 0331026338

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSQJ31Y12ZD7QJVYHX8TRH0A

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

TEKNOBIOS 5L08056646471218
TEKNOBIOS CART.HUB08056646471256
TEKNOBIOS UP08056646471171
TEKNOLINK 5L08056646471195
TEKNOLINK CART08056646471232
TEKNOLINK UP08056646471157