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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 tube FDA UDI
Device Name
TS3 - Laparoscopic Smoke evacuation tube (1 each/ 12 pcs per Case) FDA UDI
Model / Reference
TS3 FDA UDI
Description
TS3 - Laparoscopic Smoke evacuation tube (1 each/ 12 pcs per Case) FDA UDI

Identifiers

Primary DI / UDI-DI
00817325023801 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Surgical plume evacuation system tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical plume evacuation system tube

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

Similar devices

Also classified as Surgical plume evacuation system tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medimax Tech Inc.

Sources (1)

  • FDA UDI 4ff31c3d-1866-43d1-a8b2-82232f9ee633 34 fields · synced May 30, 2026