Pathfinder Endoscope Overtube

by Neptune Medical 6 variants

Ref GI 065140-2E

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	Number0850006222PATHFINDEROTHZ Basic UDI-DI 00850006222131UDI-DI	Date20 Jun 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Withdrawn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: Pathfinder Endoscope Overtube
Model / Reference: GI 065140-2E

Primary DI / UDI-DI: 00850006222131
Basic UDI-DI: 0850006222PATHFINDEROTHZ
EMDN Code: G030899 Instruments for gastro-intestinal endoscopy and eco-endoscopy, single-use - other

Device Class: Class IIa
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: US-MF-000039356
Authorised representative: Advena Limited MT-AR-000000234

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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