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CAREMED SUPPLY, INC.

Taiwan · New Taipei City

✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, South Korea, Australia — 4 overseas markets. The China NMPA lookup is still pending.

Registrations by market

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

CNChinaNMPA

pendingnot queried

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

6listed device types

Class I 2Class II 4Class III 0

plus 14 registration records and 4 510(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

25active device licences

Class II 25

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

1GMP quality-system certificates

Import 1

AUAustraliaTGA ARTG

9active ARTG entries

Class I 5IIa 4

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 States14 registration records, 4 510(k), 0 PMA, 6 excluded

Brazil0 confirmed, 3 excluded

Saudi Arabia0 confirmed, 2 excluded

Canada25 confirmed, 1 excluded

Manufacturer names merged into this page: CAREMED SUPPLY, INC.

FDA 510(k) clearances by year

12011 · K110977

12013 · K122873

12014 · K141064

12018 · K181217

FDA listed device types

Mattress, Air Flotation, Alternating Pressure 1Sleeve, Limb, Compressible 1System, Thermal Regulating 1Bed, Ac-Powered Adjustable Hospital 1Device, Transfer, Patient, Manual 1Mattress, Flotation Therapy, Non-Powered 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K181217	VesoFlow Lite DVT Compression Device	2018-08-05
US	K141064	VESOFLOW PLUS DVT COMPRESSION DEVICE	2014-12-04
US	K122873	VASOPOUSE DEEP VEIN THROMBOSIS COMPRESSION DEVICE MODEL IPCS, MODEL SQS	2013-01-15
CA	70811	AMBER ANTI-DECUBITUS MANGEMENT SYSTEM	Class II
CA	70812	TURNING SYSTEM	Class II
CA	71012	RUBY 8 AIR MATTRESS SYSTEM	Class II

CAREMED SUPPLY, INC.

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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