LoFric Insti-Cath

by Wellspect HealthCare 11 variants

Ref 40710

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	Number733338724102CX Basic UDI-DI 07333387041261UDI-DI	Date23 Mar 2026Registered	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Withdrawn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 bladder instillation
Model / Reference: 40710

Primary DI / UDI-DI: 07333387041261
Basic UDI-DI: 733338724102CX
EMDN Code: U01010501 Nelaton catheters, self-lubricating

Device Class: Class I
EU market of registration: Sweden

Manufacturer details

EUDAMED SRN: SE-MF-000026271

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Class I
Navina Consumable Set Regular

Class IIa

See all devices from Wellspect HealthCare →

Properties

Sterile
Administering Medicine

Other properties (11)

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