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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

HAEMOBAND — Class I MDR by SECURIMED

MD Atlas
SECURIMED

EUDAMED last updated this device on May 23, 2023

HAEMOBAND

37011402compressifsPH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SECURIMED
UDI-DI code: 03701140200936
Reference / catalog number: 5516

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Manufacturer information

Organization name: SECURIMED
SRN: FR-MF-000006782
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: HAEMOBAND
UDI-DI code: 03701140200936
Basic UDI-DI: 37011402compressifsPH
Reference / catalog number: 5516
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: Tampon relais compressif destiné à remplacer la compression manuelle effectuée par le secouriste en cas de forte hémorragie.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M040599HAEMOSTATIC DRESSINGS - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

HAEMOBAND37011402compressifsPHOn the market REFRICONTACTB-03701140200844On the market REFRIDOLB-03701140200110On the market 497137011402compressifsPHOn the market 486037011402compressifsPHOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.