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MULTI-MED, INC.

USA · Keene

✓ 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

7listed device types

Class I 1Class II 6Class III 0

plus 26 registration records and 8 510(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

1active device licences

Class II 1

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 States26 registration records, 8 510(k), 0 PMA, 21 excluded

Brazil0 confirmed, 2 excluded

Canada1 confirmed, 1 excluded

Manufacturer names merged into this page: MULTI-MED, INC.

FDA 510(k) clearances by year

71989 · K890424

12012 · K120195

FDA listed device types

Tube, Feeding 1Tubes, Gastrointestinal (And Accessories) 1Set, Administration, Intravascular 1Needle, Hypodermic, Single Lumen 1Catheter, Urethral 1Non-Coring (Huber) Needle 1Stethoscope, Manual 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K120195	SAFETY SUBCUTANEOUS TISSUE INFUSION SET	2012-07-06
US	K890424	ENTERAL FEEDING CONTAINER	1989-06-14
US	K890396	EXTERNAL FEEDING SET FOR PUMP USE	1989-05-23
CA	85044	SAFETY SUBCUTANEOUS TISSUE INFUSION SET	Class II

MULTI-MED, 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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