Identity
- Trade Name
- E1 electrode set (7 tips) FDA UDI
- Generic Name
- Electrosurgical system FDA UDI
- Model / Reference
- 73120185 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719873120185 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Electrosurgical system
E1 electrode set (7 tips) by Bonart Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K020080 also covers:
- ART GT E1 Electrode Set — BONART CO., LTD.
- E1 Hand Piece — BONART CO., LTD.
- E1 Handpiece (L) — BONART CO., LTD.
- E1 Handpiece (S) — BONART CO., LTD.
- E1 INDIFFERENCE PLATE ∮ 6.3mm — BONART CO., LTD.
- E1 Indiference Plate — BONART CO., LTD.
- E1 Indifference plate — BONART CO., LTD.
- ELECTROSURGERY SYSTEM — BONART CO., LTD.
- GT1 Blade Type Electrode — BONART CO., LTD.
- GT2 Small Loop Electrode — BONART CO., LTD.
- GT3 Large Loop Electrode — BONART CO., LTD.
- GT4 Fine Wire Electrode — BONART CO., LTD.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Bonart Co., Ltd.
Sources (1)
- FDA UDI 5b0f779d-ae1c-4953-86b2-c9ae7ef156d2 33 fields · synced Jun 1, 2026