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Electrosurgery System

FDA UDI

Class II (US FDA UDI)

by Bonart Co., Ltd.

Identity

Trade Name
ELECTROSURGERY SYSTEM FDA UDI
Generic Name
Electrosurgical system FDA UDI
Model / Reference
ART-E1 FDA UDI

Identifiers

Primary DI / UDI-DI
04719873120048 FDA UDI
510(k) Number
K020080 FDA UDI
FDA Product Code
EKZ FDA UDI
GMDN Term
Electrosurgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4920 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical system

Electrosurgery System by Bonart Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bonart Co., Ltd.

Sources (1)

  • FDA UDI 127395a3-2ebf-4d9b-a753-b262ba1f56b3 33 fields · synced May 30, 2026