Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014572985

FEI Number

3014572985

Entity Name

C MEDICAL SUPPLIES

City/State/Country

Ajax Ontario, CA

Establishment Address

54 Marshall Cres, Ajax Ontario L1T 2N4, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

C Medical Supplies (Owner Number: 10087346)

Owner / Operator Contact Address

54 Marshall Cres, Ajax, CA-ON L1T 2N4, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P160026

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPP	Stretcher, Hand-Carried	General Hospital	Class 1	880.6900	2023-08-03
MKJ	Automated External Defibrillators (Non-Wearable)	Cardiovascular	Class 3	870.5310	2023-02-15

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

C Medical Supplies

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-2010	Philips Healthcare Inc.	3	HeartStart MRx (M3535A/M3536A) Defibrillator/Monitor. The HeartStart MRx/MRxE is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician.
Z-0004-06	Medtronic Emergency Response Systems, Inc.	3	Hard shell carry case for the LIFEPAK 500 AED.
Z-0004-2017	Leonhard Lang Medizintechnik GmbH Archenweg 56 Innsbruck Austria	3	Skintact Electrodes for Defibrillation, DF29N. Product Usage: Multifunction electrode for external defibrillation, pacing, cardioversion, and monitoring. The device is non-sterile and for single use only.
Z-0005-06	Medtronic Emergency Response Systems, Inc.	3	Hard shell carry case for the LIFEPAK CR Plus.
Z-0011-2013	Philips Healthcare Inc.	3	Philips HeartStart XL M4735A Defibrillator/Monitors, used with the M3516A batteries The Heart Start XL Defibrillator/Monitor is a fully featured, defibrillator intended for use by qualified medical personnel, trained in either Advanced Cardiac Life Support or in the operation of the device, in a hospital environment.

Similar Registrations

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3038623066	WUYI KINDA INDUSTRY & TRADE CO., LTD	JINHUA Zhejiang, CN
3043654660	HEBEI JIEDE MEDICAL EQUIPMENT CO., LTD.	Hengshui Hebei, CN
3015775888	BETTER TEXTILE GARMENT COMPANY LIMITED	Da Nang, VN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014572985. Last updated year: 2026. Please use registration number 3014572985 when referencing this establishment in official correspondence.