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T2 Small loop electrode

FDA UDI

Class II (US FDA UDI)

by Bonart Co., Ltd.

Identity

Trade Name
T2 Small loop electrode FDA UDI
Generic Name
Electrosurgical system FDA UDI
Model / Reference
T2 FDA UDI

Identifiers

Primary DI / UDI-DI
04719873120475 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical system

T2 Small loop electrode 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 1c86e5e5-ed45-4e8a-bde4-35912718d285 33 fields · synced Jun 8, 2026