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AincA®

FDA UDI

Class II (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name
AincA® FDA UDI
Generic Name
Airway pressure monitor, non-powered FDA UDI
Device Name
Manometer, Pressure, -40 to +80 cm H2O, 1/4" NPT-M Top-Mount, 2.5"Dia, Front Zero-Adjust FDA UDI
Model / Reference
00-199-TOP FDA UDI
Description
Manometer, Pressure, -40 to +80 cm H2O, 1/4" NPT-M Top-Mount, 2.5"Dia, Front Zero-Adjust FDA UDI

Identifiers

Catalog Number
00-199-TOP FDA UDI
Primary DI / UDI-DI
B00500199TOP0 FDA UDI
FDA Product Code
CAP FDA UDI
GMDN Term
Airway pressure monitor, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2600 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: Airway pressure monitor, non-powered

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

Similar devices

Also classified as Airway pressure monitor, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6bda812-0ba0-4157-9c57-40c2d3ed6edf 35 fields · synced May 30, 2026