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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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HOMECARE — 17 UDI-DI variants, MDR (SAFTE S.r.l.)

MD Atlas
SAFTE S.r.l.

Data from EUDAMED, last updated May 31, 2026

HOMECARE

805390450HOMECAREW8

17 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: SAFTE S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805390450HOMECAREW8
Device name: —
Device model: HOMECARE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: SAFTE S.r.l.
SRN: IT-MF-000011223
Country: Italy
Email: sara.santoriello@safte.it
Phone: +390114038111

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01KRGYNFAYAK6ARBQNS2MNPZX7

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

7013BN08056045439925
7033BN08056045439963
111208053904509294
7012BN08056045439956
7030BN08056045439970
7031BN08056045439987
7010BN08056045439932
7011BN08056045439949
7032BN08056045439994
111108056045439796
7001BN08056045439819
7000BN08056045439802
7004BN08056045439840
7005BN08056045439857
7002BN08056045439826
7006BN08056045439864
7003BN08056045439833