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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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COTOVELO ELÁSTICO — 10 UDI-DI variants, MDR

MD Atlas
P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA

Data from EUDAMED, last updated May 30, 2026

COTOVELO ELÁSTICO

560080609COSUP8W

10 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: P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 560080609COSUP8W
Device name: COTOVELO ELÁSTICO
Device model: 100/170
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA
SRN: PT-MF-000010370
Country: Portugal
Email: lbrandao@peeth.pt
Phone: +351 256 422 282

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ7QCN4PF77R5QQD9TAPET88

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

100/105600806090097
100/205600806090103
100/305600806090110
100/405600806090127
100/505600806090134
100/605600806090141
170/L05600806090240
170/M05600806090233
170/S05600806090226
170/XL05600806090257