MediMax Tech

FDA UDI

Class II (US FDA UDI)

by Medimax Tech Inc.

Identity

Trade Name: MediMax Tech FDA UDI
Generic Name: Surgical plume evacuation system FDA UDI
Device Name: EcoEvRNHT-10 Standard Smoke Evacuation Pencil with Insulated 2.5" Ceramic Coated Non Stick Blade with Holster; 10' Cable - Single Pack FDA UDI
Model / Reference: EcoEvRNHT-10 FDA UDI
Description: EcoEvRNHT-10 Standard Smoke Evacuation Pencil with Insulated 2.5" Ceramic Coated Non Stick Blade with Holster; 10' Cable - Single Pack FDA UDI

Identifiers

Primary DI / UDI-DI: 00817325023078 FDA UDI
510(k) Number: K092732 FDA UDI
K143103 FDA UDI
FDA Product Code: GEI FDA UDI
GMDN Term: Surgical plume evacuation system 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical return electrode, single-use Surgical plume evacuation system

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

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Cleared under the same submission

K092732 also covers:

K143103 also covers:

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: Medimax Tech Inc.

Sources (1)

FDA UDI ce28d6e2-5997-478c-9d90-aabdfa802f41 35 fields · synced Jun 8, 2026