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Airflow Thermistor PediatricSleepmate

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
Airflow Thermistor PediatricSleepmate FDA UDI
Generic Name
Polysomnograph FDA UDI
Device Name
Thermistor Airflow Ped FDA UDI
Model / Reference
1420402 FDA UDI
Description
Thermistor Airflow Ped FDA UDI

Identifiers

Catalog Number
1420402 FDA UDI
Primary DI / UDI-DI
05707480043118 FDA UDI
510(k) Number
K903300 FDA UDI
FDA Product Code
BZQ FDA UDI
GMDN Term
Polysomnograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Commercial Distribution
Not 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

Airflow Thermistor PediatricSleepmate by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI ed0e6c00-68f4-47cd-9455-8dd5a43e106e 37 fields · synced May 30, 2026