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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

HARRT PRO SB — Class I MDR by Oy Klippan Ab

MD Atlas
Oy Klippan Ab

EUDAMED last updated this device on Mar 20, 2026

HARRT PRO SB

641764002756B6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Oy Klippan Ab
UDI-DI code: 06417640027566
Reference / catalog number: HA-PV HARRT Pro SB - SAFETY BELT

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Manufacturer information

Organization name: Oy Klippan Ab
SRN: FI-MF-000052644
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW999
Critical warning - Inspect harness before each use - Do not use if product or components damaged.
CW018
EUDAMED did not publish a description for this code.

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: HARRT PRO SB
UDI-DI code: 06417640027566
Basic UDI-DI: 641764002756B6
Reference / catalog number: HA-PV HARRT Pro SB - SAFETY BELT
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: HARRT Pro SB - SAFETY BELT
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050199PATIENT TRANSFER STRETCHERS - 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

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.

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