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Smoke Filter with Tube

FDA UDI

Class II (US FDA UDI)

by Armm Inc.

Identity

Trade Name
Smoke Filter with Tube FDA UDI
Generic Name
Laparoscopic plume filter FDA UDI
Device Name
Laparoscopic Smoke Filtration System FDA UDI
Model / Reference
301-S400 FDA UDI
Description
Laparoscopic Smoke Filtration System FDA UDI

Identifiers

Primary DI / UDI-DI
10850082007094 FDA UDI
FDA Product Code
FYD FDA UDI
GMDN Term
Laparoscopic plume filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5070 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic plume filter

Smoke Filter with Tube by Armm Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic plume filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Armm Inc.

Sources (1)

  • FDA UDI fb61151d-ee45-4b0c-8e5e-1505d82f9f61 34 fields · synced May 30, 2026