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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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Organization name
UDI-DI code
Reference / catalog number

Jeringa de plástico — Class I MDR by METALGAR, S.L.

MD Atlas
METALGAR, S.L.

EUDAMED last updated this device on Oct 9, 2024

Jeringa de plástico

8437027121PS000403E

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: METALGAR, S.L.
UDI-DI code: 08437027121043
Reference / catalog number: Jeringa de plástico

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Manufacturer information

Organization name: METALGAR, S.L.
SRN: ES-MF-000005319
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08437027121043
Basic UDI-DI: 8437027121PS000403E
Reference / catalog number: Jeringa de plástico
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: JERINGA DE PLÁSTICO, 1-5ml CON DIVISIÓN DE ESCALA DE 0,5ml
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5 MU03

EMDN nomenclature code(s)

V0380DEVICES WITH MEASURING FUNCTIONS - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

Certificate health across this manufacturer's portfolio.

2026 PR 0074Issued
Quality assuranceNotified body: 0318Expiry: Feb 16, 2031