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LAERDAL MEDICAL CANADA LTD.

Canada · Toronto

✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

9listed device types

Class I 5Class II 4Class III 0

plus 12 registration records and 20 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

13active device licences

Class II 11Class III 2

22 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States12 registration records, 20 510(k), 0 PMA, 4 excluded

Canada13 confirmed, 0 excluded

Manufacturer names merged into this page: LAERDAL MEDICAL A/S · LAERDAL MEDICAL AS · LAERDAL MEDICAL CANADA LTD.

FDA 510(k) clearances by year

11982

11984

11986

11988

11990

11993

11995

31996

11999

12000

12003

12012

22015

22018

12024

12025

FDA listed device types

showing 8 of 9

Aid, Cardiopulmonary Resuscitation 1Ventilator, Emergency, Manual (Resuscitator) 1Attachment, Breathing, Positive End Expiratory Pressure 1Monitor, Airway Pressure (Includes Gauge And/Or Alarm) 1Stretcher, Hand-Carried 1Orthosis, Truncal/Orthosis, Limb 1Device, Prosthesis Alignment 1Mask, Oxygen 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K251631	The BAG manual resuscitator and accessories	2025-11-24
US	K232111	NeoBeat, NeoBeat Mini	2024-06-25
US	K183348	Reusable Silicone Cover CPRmeter 2	2018-12-17
CA	19301	TRACHLIGHT STYLET AND TRACHEAL LIGHT WAND	Class II
CA	21437	HEARTSTART 4000 DEFIBRILLATOR	Class III
CA	26896	LAERDAL HEARTSTART FR2	Class III

LAERDAL MEDICAL CANADA LTD.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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