← Back to catalogue

Venistar

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 7-VENI0070N

by STARmed Co., Ltd.

Identity

Trade Name
VENISTAR EUDAMEDFDA UDI
Generic Name
Peripheral vascular radio-frequency ablation catheter FDA UDI
Device Name
VENISTAR EUDAMED
Model / Reference
7-VENI0070N EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08809306767875 EUDAMEDFDA UDI
Basic UDI-DI
880930676VENISTAR_E8G EUDAMED
B-08809306767875 EUDAMED
510(k) Number
K222997 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
K0201010301 OPEN ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED
GMDN Term
Peripheral vascular radio-frequency ablation catheter FDA UDI

Classification

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

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Venistar by Starmed Co., Ltd — Class IIb — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
STARmed Co., Ltd.
EUDAMED SRN
KR-MF-000008605
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (3)

  • EUDAMED 2a956aaf-7398-4fba-9cdf-2532ab413827 61 fields · synced Aug 2, 2026
  • EUDAMED 0580d9f9-b027-43c4-ab0e-f22c4af49ace 61 fields · synced May 18, 2026
  • FDA UDI 29aa678d-7699-4228-9a60-4672675a1fe7 33 fields · synced May 29, 2026