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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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PEROMED 38/40 SINISTRO — 1 UDI-DI variant, MDR (A3-MED SRL)

MD Atlas
A3-MED SRL

Data from EUDAMED, last updated May 31, 2026

PEROMED 38/40 SINISTRO

080548902002713840L9N

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: A3-MED SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 080548902002713840L9N
Device name: PEROMED 38/40 SINISTRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: A3-MED SRL
SRN: IT-MF-000011063
Country: Italy
Email: info@a3med.it
Phone: +390514125204

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KRX01JPNTAM5RYQZAGAYKMPT

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

0140900L08054890200271