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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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Spikes — 14 UDI-DI variants, MDR (Produtos Médicos Hospitalares, SA)

MD Atlas
Produtos Médicos Hospitalares, SA

Data from EUDAMED, last updated May 30, 2026

Spikes

560771680395

14 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

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 560771680395
Device name: Spikes
Device model: 803.4512
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

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ7N3443R02B7YFRRJN5HNK3

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

803.245705607716024570
803.441805607716044189
803.451405607716045148
803.451505607716045155
803.198105607716019811
803.451305607716045131
803.217905607716021791
803.065805607716006583
803.451205607716045124
803.197405607716019743
803.439305607716043939
803.242905607716024297
803.065605607716006569
803.065705607716006576