Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Extension sets — 901 UDI-DI variants, MDR

MD Atlas
Produtos Médicos Hospitalares, SA

Data from EUDAMED, last updated May 31, 2026

Extension sets

560771630086

901 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Produtos Médicos Hospitalares, SA

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 560771630086
Device name: Extension sets
Device model: 313.1978
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Produtos Médicos Hospitalares, SA
SRN: PT-MF-000007631
Country: Portugal
Email: cristina.coelho@pmh.pt
Phone: +351263650680

Variants by status

UDI-DI variants

901 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KQ7CXNJ0W5VZ760ABWYA5VX7

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

303.211605607716021166
307.043705607716004374
301.452005607716045209
307.476805607716047685
302.038405607716003841
306.498905607716049894
307.170605607716017060
306.235005607716023504
313.472705607716047272
301.032305607716003230
313.070905607716007092
311.163505607716016353
AMT043005607716104302
309.470105607716047012
306.253505607716025355
AMT0114K05607716101875
307.505005607716050500
309.390805607716039086
306.393105607716039314
302.364405607716036443
308.047205607716004725
310.492205607716049221
302.350105607716035019
309.379605607716037969
312.376405607716037648