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CROSS PROTECTION

Malaysia
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 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
4listed device types
Class I 3Class II 1Class III 0
plus 6 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
11registered devices
Class I 11
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
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 States6 registration records, 1 510(k), 0 PMA, 15 excluded
Brazil11 confirmed, 3 excluded
Manufacturer names merged into this page: CROSS PROTECTION M SDN BHD · CROSS PROTECTION · CROSS PROTECTION (M) SDN. BHD. · CROSS PROTECTION (M) SDN.BHD
Same-named companies — This database also contains companies with near-identical names: CROSS PROTECTION (M) SDN. BHD.. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
Malaysia

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12022 · K212273

FDA listed device types

Latex Patient Examination Glove 1Mouthpiece, Saliva Ejector 1Accessory, Surgical Apparel 1Mask, Surgical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK212273Cross Protection ResQ300 Plus Surgical Face Mask2022-08-17
BR80044549001DRENO DE SUCÇÃO DESCARTÁVEL LAGROTTA AZZURRAClass I
BR10223060050Máscara Facial Cross ProtectionClass I
BR10223060047Touca Cross ProtectionClass I

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