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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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Autoreg. MICROFIBRA — 60 UDI-DI variants, MDR

MD Atlas
NEW MEDICAL SERVICE SRL

Data from EUDAMED, last updated May 31, 2026

Autoreg. MICROFIBRA

80536857267290442RF

60 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: NEW MEDICAL SERVICE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80536857267290442RF
Device name: Autoreg. MICROFIBRA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEW MEDICAL SERVICE SRL
SRN: IT-MF-000034543
Country: Italy
Email: info@flebysan.it
Phone: +39425474993

Variants by status

UDI-DI variants

60 UDI-DI variants

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Applied filters

basicUdiUlid01K4M38ZN51DZ1B8QQ3K23718B

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

805368572672908053685726729
805368572702308053685727023
805368572705408053685727054
805368572699608053685726996
805368572704708053685727047
805368572707808053685727078
805368572701608053685727016
805368572703008053685727030
805368572706108053685727061
805368572700908053685727009

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