hi-slip plus

by Wellspect HealthCare 61 variants

Ref TRHSPM4010B

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number733338724101CV Basic UDI-DI 07333387001296UDI-DI	Date14 Feb 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Single use hydrophilic urinary catheter for intermittent urinary catheterization
Model / Reference: TRHSPM4010B

Primary DI / UDI-DI: 07333387001296
Basic UDI-DI: 733338724101CV
EMDN Code: U01010501 Nelaton catheters, self-lubricating

Device Class: Class I
EU market of registration: Denmark

Manufacturer details

EUDAMED SRN: SE-MF-000026271

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Properties

Sterile

Other properties (12)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No