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AincA®

FDA UDI

Class II (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name
AincA® FDA UDI
Generic Name
Anaesthetic gas scavenging unit FDA UDI
Device Name
Valve, Scavenging, 0-60 cmH2O True APL Pop-Off (not LeakTight), 90°, 3/4"-20 x 19mmM, Chrome Brass FDA UDI
Model / Reference
00-118 FDA UDI
Description
Valve, Scavenging, 0-60 cmH2O True APL Pop-Off (not LeakTight), 90°, 3/4"-20 x 19mmM, Chrome Brass FDA UDI

Identifiers

Catalog Number
00-118 FDA UDI
Primary DI / UDI-DI
B005001180 FDA UDI
FDA Product Code
CBN FDA UDI
GMDN Term
Anaesthetic gas scavenging unit 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthetic gas scavenging unit

AincA® by Anesthesia Associates, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthetic gas scavenging unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anesthesia Associates, Inc.

Sources (1)

  • FDA UDI abecfbd6-a35e-445e-a356-417924b848cc 35 fields · synced May 30, 2026