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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
Scavenging Manifold, 19mmM, 1/4" Vacuum Adjust Valve, Pos/Neg Relief Valves, Bag Mount, Mount Strip FDA UDI
Model / Reference
00-117 FDA UDI
Description
Scavenging Manifold, 19mmM, 1/4" Vacuum Adjust Valve, Pos/Neg Relief Valves, Bag Mount, Mount Strip FDA UDI

Identifiers

Catalog Number
00-117 FDA UDI
Primary DI / UDI-DI
B005001170 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 5716dbdb-16e0-43e8-a435-fa59d497d3ba 35 fields · synced Jun 8, 2026