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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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SEPARADOR DEDOS — 3 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

SEPARADOR DEDOS

560080609SEPODAF

3 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: 560080609SEPODAF
Device name: SEPARADOR DEDOS
Device model: 1031
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KQ7PJ41AF106MG2G35X94BMV

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

1031/G05600806090158
1031/M05600806090165
1031/P05600806090172