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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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Bote 3L — 3 UDI-DI variants, IVDR

MD Atlas
Plasticerveira - Transformação de Plástico, Lda

Data from EUDAMED, last updated May 30, 2026

Bote 3L

5600299202FA00039KS

3 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: Plasticerveira - Transformação de Plástico, Lda

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5600299202FA00039KS
Device name: Bote 3L
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Plasticerveira - Transformação de Plástico, Lda
SRN: PT-MF-000019369
Country: Portugal
Email: qualidade@cplas.pt
Phone: +351251104893

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G3RVPQJC5YCKHKRQ34JSZ4J3

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

PL03-0163-04 05600299202083
PL03-0162-04 05600299202076
PL03-0163-SC05600299202090