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Automatic Vacuum Switch Avs

FDA UDI

Class II (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name
AUTOMATIC VACUUM SWITCH AVS FDA UDI
Generic Name
Anaesthesia workstation gas scavenger FDA UDI
Device Name
AUTOMATIC VACCUM SWITCH SYSTEM FDA UDI
Model / Reference
AVS-5000 FDA UDI
Description
AUTOMATIC VACCUM SWITCH SYSTEM FDA UDI

Identifiers

Primary DI / UDI-DI
00816711020295 FDA UDI
510(k) Number
K981754 FDA UDI
FDA Product Code
CBN FDA UDI
GMDN Term
Anaesthesia workstation gas scavenger FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5430 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

No

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

No

FDA UDI

Category: Anaesthesia workstation gas scavenger

Automatic Vacuum Switch Avs by Parker Hannifin Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia workstation gas scavenger.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af66eb56-c2d1-4bf5-9619-93cc9e37e259 34 fields · synced May 30, 2026