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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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ANAPAT Prefilled, contentores… — 6 UDI-DI variants, IVDR

MD Atlas
ESTERIPLAS- PRODUTOS PARA A AREA DA SAUDE, LDA

Data from EUDAMED, last updated May 30, 2026

ANAPAT Prefilled, contentores pré-cheios com Formol a 10% tamponado

56083842800544Z

6 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: ESTERIPLAS- PRODUTOS PARA A AREA DA SAUDE, LDA

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 56083842800544Z
Device name: ANAPAT Prefilled, contentores pré-cheios com Formol a 10% tamponado
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: ESTERIPLAS- PRODUTOS PARA A AREA DA SAUDE, LDA
SRN: PT-MF-000033228
Country: Portugal
Email: geral@esteriplas.mail.pt
Phone: +351 256 330 350

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JQVKZ46DZ5QB1JXEP3TE74MP

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

10050028005905608384014924
10050028005605608384014894
10050028005705608384014900
10050028005405608384014870
10050028005805608384014917
10050028005505608384014887