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Premier Evacuator 220V Air Filtration System

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Premier Evacuator 220V Air Filtration System FDA UDI
Generic Name
Surgical plume evacuation system FDA UDI
Device Name
Premier Evacuator 220V Air Filtration System. Contains one Premier Evacuator 220V unit, one detachable cord, and Disposable Filter Pack (5 filters - reorder number 9006290). FDA UDI
Model / Reference
9006298 FDA UDI
Description
Premier Evacuator 220V Air Filtration System. Contains one Premier Evacuator 220V unit, one detachable cord, and Disposable Filter Pack (5 filters - reorder number 9006290). FDA UDI

Identifiers

Catalog Number
9006298 FDA UDI
Primary DI / UDI-DI
D69190062980 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

Premier Evacuator 220V Air Filtration System by Dermatologic Lab And Supply, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f25a803a-60b2-4843-ae0c-67d194f0af1d 34 fields · synced Jun 8, 2026