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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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Reusable Blood Pressure Connection… — 5 UDI-DI variants, MDR

MD Atlas
NISSHA MEDICAL TECHNOLOGIES SAS

Data from EUDAMED, last updated May 19, 2026

Reusable Blood Pressure Connection Cables

037005063Pressure-CableV3

5 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: NISSHA MEDICAL TECHNOLOGIES SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 037005063Pressure-CableV3
Device name: Reusable Blood Pressure Connection Cables
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: NISSHA MEDICAL TECHNOLOGIES SAS
SRN: FR-MF-000009791
Country: France
Email: regulatory@nisshamedical.com
Phone: +33139726666

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GHB89AG6Y3QGTNHJZ2RDJN6R

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

8876003700506303564
8822503700506308781
8812003700506308941
8816203700506308910
8811503700506308958