SCANLAN® Monopolar Probe 1001-3200

by Scanlan International Inc

Ref 3003-174

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD EUDAMED	NumberB-00846159021820 Basic UDI-DI 00846159021820UDI-DI	Date18 May 2026Registered	StatusActive
United States	GUDID listing GUDID	Number00846159021820 UDI-DI	Date20 Jun 2016Listed	StatusListed GUDID: in commercial distribution

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

2 jurisdictions

Active
Expiring
Withdrawn
Listed
Not covered

European Union CE/MDD Active
United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name: SCANLAN® Monopolar Probe
Generic Name: Open-surgery electrosurgical electrode, monopolar, reusable
Device Name: SCANLAN® Probe
Model / Ref / Catalog: 3003-174 EUDAMED
1001-3200 GUDID

Primary DI / UDI-DI: 00846159021820 EUDAMED
00846159031805 GUDID
Basic UDI-DI: B-00846159021820
FDA Product Code: GEI
EMDN Code: L031102 Exploration probes, reusable
GMDN Term: Open-surgery electrosurgical electrode, monopolar, reusable

Device Class: Class I EUDAMED
Class II GUDID
Regulation Number: 878.4400
EU market of registration: Netherlands
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

Field	EUDAMED	GUDID
Model / Reference	EUDAMED 3003-174	GUDID 1001-3200
Primary DI / UDI-DI	EUDAMED 00846159021820	GUDID 00846159031805
Device Class	EUDAMED Class I	GUDID Class II

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Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (21)

Sterile: No
Single Use: No
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
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No