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

H7264003005607716126434
304.082905607716008297
301.243705607716024372
309.421605607716042161
306.501905607716050197
AMT006105607716100618
303.039205607716003926
309.153105607716015318
306.377705607716037778
AMT035505607716103558
301.497305607716049733
AMT004505607716100458
301.276205607716027625
307.046805607716930093
306.189305607716018937
AMT0047RV05607716103015
301.276305607716027632
301.458805607716045889
303.002805607716000284
AMT015605607716101561
313.197905607716019798
AMT002505607716100250
AMT002605607716100267
307.196305607716019637
311.148905607716014892

1 2 3 4 5