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NS 30-PBR Negative Inspiratory Force (NIF) Meter

FDA UDI

Class II (US FDA UDI)

by Instrumentation Industries, Incorporated

Identity

Trade Name
NS 30-PBR Negative Inspiratory Force (NIF) Meter FDA UDI
Generic Name
Airway pressure monitor, non-powered FDA UDI
Device Name
The Instrumentation Industries, Inc. NS Series Negative Inspiratory Force (NIF) Meters are devices used to measure and monitor patient inspiratory effort. During use the NIF Meter is attached to the patient airway at a point that provides optimal readings of patient respiratory effort. Federal law restricts these devices to sale by or on the order of a physician. FDA UDI
Model / Reference
NS 30-PBR FDA UDI
Description
The Instrumentation Industries, Inc. NS Series Negative Inspiratory Force (NIF) Meters are devices used to measure and monitor patient inspiratory effort. During use the NIF Meter is attached to the patient airway at a point that provides optimal readings of patient respiratory effort. Federal law restricts these devices to sale by or on the order of a physician. FDA UDI

Identifiers

Catalog Number
NS 30-PBR FDA UDI
Primary DI / UDI-DI
M996NS30PBR0 FDA UDI
510(k) Number
K081693 FDA UDI
FDA Product Code
BXR FDA UDI
GMDN Term
Airway pressure monitor, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1780 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

No

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

NS 30-PBR Negative Inspiratory Force (NIF) Meter by Instrumentation Industries, Incorporated — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Airway pressure monitor, non-powered.

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 ef1f72ad-6391-4a36-a44d-c3784eb77b94 36 fields · synced May 30, 2026