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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

BHL-InfuCare line — Class I MDR by BHL-Medical, Indústria…

MD Atlas
BHL-Medical, Indústria de Produtos Hospitalares, lda

EUDAMED last updated this device on Apr 3, 2025

BHL-InfuCare line

56009888TF005L4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BHL-Medical, Indústria de Produtos Hospitalares, lda
UDI-DI code: 05600988816119
Reference / catalog number: 3302009

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Manufacturer information

Organization name: BHL-Medical, Indústria de Produtos Hospitalares, lda
SRN: PT-MF-000002811
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

ITD 1450490 1Supplemented
Quality assuranceNotified body: 1936Expiry: Jan 13, 2030

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
No contra indications are identified. There’s a high level of protection to the health and safety of patients when device is used as intended.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement	Jan 15, 2025	Dec 31, 2050

Device identification

Trade name: BHL-InfuCare line
UDI-DI code: 05600988816119
Basic UDI-DI: 56009888TF005L4
Reference / catalog number: 3302009
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: Intended for therapeutic administration of infusion solutions when connected to a needle or catheter.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

A03020199EXTENSIONS - OTHER

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

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