← Back to catalogue

Pro-Tech

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Pro-Tech FDA UDI
Generic Name
Airway temperature monitoring system FDA UDI
Device Name
Pro-Tech Airflow Sensor Thermistor Pediatric 1 Alice 3 FDA UDI
Model / Reference
AIRFLOW SENSOR THERMISTOR FDA UDI
Description
Pro-Tech Airflow Sensor Thermistor Pediatric 1 Alice 3 FDA UDI

Identifiers

Catalog Number
P1298 FDA UDI
Primary DI / UDI-DI
00606959010215 FDA UDI
510(k) Number
K960851 FDA UDI
FDA Product Code
BZQ FDA UDI
GMDN Term
Airway temperature monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 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

Yes

FDA UDI

Category: Airway temperature monitoring system

Pro-Tech by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway temperature monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI f2d50c12-847d-4417-ac45-80d1ade202fe 37 fields · synced May 30, 2026