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RapidVac

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
RapidVac FDA UDI
Generic Name
Surgical plume evacuation system FDA UDI
Device Name
Smoke Evacuator 110V FDA UDI
Model / Reference
SE3690ZD FDA UDI
Description
Smoke Evacuator 110V FDA UDI

Identifiers

Primary DI / UDI-DI
10884521134140 FDA UDI
510(k) Number
K142335 FDA UDI
K980915 FDA UDI
FDA Product Code
FYD FDA UDI
GMDN Term
Surgical plume evacuation system 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical plume evacuation system

RapidVac by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system.

Cleared under the same submission

K142335 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 180276f1-16c3-4666-b382-9d8db4f11945 36 fields · synced May 30, 2026