← Back to catalogue

Bipolar Turbinate Cautery Electrode

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref I6/JXE

by Cynosure LLC

Identity

Trade Name
Bipolar Turbinate Cautery Electrode EUDAMEDFDA UDI
Generic Name
Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
Bipolar Turbinate Cautery Electrode EUDAMED
BAYONETTE TURBINATE ELECTRODE WITH HP FDA UDI
Model / Reference
I6/JXE EUDAMEDFDA UDI
Description
BAYONETTE TURBINATE ELECTRODE WITH HP FDA UDI

Identifiers

Catalog Number
I6/JXE FDA UDI
Primary DI / UDI-DI
00841494102043 EUDAMEDFDA UDI
Basic UDI-DI
B-00841494102043 EUDAMED
510(k) Number
K071343 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L180301 OPEN ELECTROSURGERY HANDPIECES, REUSABLE EUDAMED
GMDN Term
Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Bipolar Turbinate Cautery Electrode by Cynosure, LLC — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cynosure LLC
EUDAMED SRN
US-MF-000010200
Authorised Representative
Cynosure B.V. NL-AR-000009566

Sources (2)

  • EUDAMED 2040c885-9089-444c-b172-3cf3671a3e0b 61 fields · synced Jul 17, 2026
  • FDA UDI 78d3664b-e8c3-4d2d-94e8-ceddc2eab975 35 fields · synced May 30, 2026