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AincA®

FDA UDI

Class II (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name
AincA® FDA UDI
Generic Name
Breathing circuit gas-flow sensor, reusable FDA UDI
Device Name
Respirometer, Analog, Case, w/ Foam Insert Set FDA UDI
Model / Reference
00-306 FDA UDI
Description
Respirometer, Analog, Case, w/ Foam Insert Set FDA UDI

Identifiers

Catalog Number
00-306 FDA UDI
Primary DI / UDI-DI
B005003060 FDA UDI
FDA Product Code
BZK FDA UDI
GMDN Term
Breathing circuit gas-flow sensor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1850 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: Breathing circuit gas-flow sensor, reusable

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

Similar devices

Also classified as Breathing circuit gas-flow sensor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8e1e53da-d81d-41c5-9739-f844b215af15 35 fields · synced Jun 8, 2026