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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. 12 P. APERTA — 8 UDI-DI variants, MDR

MD Atlas
NEW MEDICAL SERVICE SRL

Data from EUDAMED, last updated May 30, 2026

AUTOREG. 12 P. APERTA

80536857214100108GW

8 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: 80536857214100108GW
Device name: AUTOREG. 12 P. APERTA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 10, 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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JXCFK4V0AXJGA3WHQFBSZK0T

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

805368572141008053685721410
805368572142708053685721427
805368572143408053685721434
805368572144108053685721441
805368572145808053685721458
805368572146508053685721465
805368572147208053685721472
805368572148908053685721489