← Back to catalogue

MediMax Tech

FDA UDI

Class II (US FDA UDI)

by Medimax Tech Inc.

Identity

Trade Name
MediMax Tech FDA UDI
Generic Name
Electrocautery system electrode FDA UDI
Device Name
Ball Electrodes RE53: Stainless Steel, 5mm ball, 5.3'', ESU Pencil Accessories FDA UDI
Model / Reference
Ball Electrodes RE53 FDA UDI
Description
Ball Electrodes RE53: Stainless Steel, 5mm ball, 5.3'', ESU Pencil Accessories FDA UDI

Identifiers

Primary DI / UDI-DI
00817325022439 FDA UDI
510(k) Number
K143103 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrocautery system electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocautery system electrode

MediMax Tech by Medimax Tech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocautery system electrode.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Medimax Tech Inc.

Sources (1)

  • FDA UDI fa3dbead-6be0-466f-9960-ff5d73525194 35 fields · synced May 30, 2026