Home›Singapore›Medipurpose Pte. , Ltd.

Medipurpose Pte. , Ltd.

Singapore · Singapore

✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Canada, Singapore, Australia — 5 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

10listed device types

Class I 6Class II 3Class III 0unclassified 1

plus 13 registration records and 5 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

2registered devices

Class II 2

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

0active device licences

4 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

2device registrations

CLASS B 2

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

1active ARTG entries

IIa 1

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 States13 registration records, 5 510(k), 0 PMA

Brazil2 confirmed, 0 excluded

Manufacturer names merged into this page: MEDIPURPOSE PTE. LTD. · MEDIPURPOSE PTE LTD. · MEDIPURPOSE PTE. LTD · MEDIPURPOSE Pte Ltd

FDA 510(k) clearances by year

22010 · K101145

12011 · K110062

12013 · K130132

12022 · K222224

FDA listed device types

showing 8 of 10

Multiple Use Blood Lancet For Single Patient Use Only 1Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature 1Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature 1Dressing, Wound, Occlusive 1Handle, Scalpel 1Blade, Scalpel 1Dressing, Wound, Hydrophilic 1Gauze / Sponge,Nonresorbable For External Use 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K222224	SurgiLance® Safety Lancet	2022-09-22
US	K130132	BABYLANCE HEEL INCISION DEVICE	2013-02-11
US	K110062	MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG	2011-09-01
BR	10230739003	surgilance	Class II
BR	80535249001	LANCETAS MediPurpose	Class II

Medipurpose Pte. , Ltd.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

Similar companies