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MediMax Tech

FDA UDI

Class I (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
ASF3: Laparoscopic Smoke Evacuation, ActiveVC, Active type with Volume Control, Filter and Fluid Trap - (1 pc per pack/ 10 pcs per box) FDA UDI
Model / Reference
ASF3 FDA UDI
Description
ASF3: Laparoscopic Smoke Evacuation, ActiveVC, Active type with Volume Control, Filter and Fluid Trap - (1 pc per pack/ 10 pcs per box) FDA UDI

Identifiers

Primary DI / UDI-DI
00817325023771 FDA UDI
FDA Product Code
NKC FDA UDI
GMDN Term
Surgical plume evacuation system tube FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1730 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 I — 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 f4f50e5e-869b-4ce5-a790-b0851116c929 34 fields · synced Jun 6, 2026