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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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BHL-Hiflow — 7 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 30, 2026

BHL-Hiflow

56009888TD001SMH5

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BHL-Medical, Indústria de Produtos Hospitalares, lda

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 56009888TD001SMH5
Device name: —
Device model: BHL-Hiflow
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: BHL-Medical, Indústria de Produtos Hospitalares, lda
SRN: PT-MF-000002811
Country: Portugal
Email: geral@bhl-medical.com
Phone: +351 219821694

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KN2D3HBGEAB3B5HPEDNQF53K

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

BHL-Hiflow05600988818601
BHL-Hiflow05600988817673
BHL-Hiflow05600988813576
BHL-Hiflow05600988817680
BHL-Hiflow05600988813538
BHL-Hiflow05600988817758
BHL-Hiflow05600988817741