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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

WANW0001 — Class I MDD by Sensotrend Oy

MD Atlas
Sensotrend Oy

EUDAMED last updated this device on Dec 1, 2021

WANW0001

B-FIMF000000500WANW00019H

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Sensotrend Oy
UDI-DI code: D-FIMF000000500WANW00019H
Reference / catalog number: WANW0001

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Manufacturer information

Organization name: Sensotrend Oy
SRN: FI-MF-000000500
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: D-FIMF000000500WANW00019H
Basic UDI-DI: B-FIMF000000500WANW00019H
Reference / catalog number: WANW0001
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

SDP00001B-FIMF000000500SDP00001UDOn the market SCP00001B-FIMF000000500SCP00001TUOn the market SUP00001B-FIMF000000500SUP000015HOn the market SC000001B-FIMF000000500SC000001F9On the market SCC00001B-FIMF000000500SCC00001NKOn 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.