HomeJapanSAN-M PACKAGE CO., LTD.

SAN-M PACKAGE CO., LTD.

Japan · Shimada-City Shizuoka
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Taiwan, Australia — 3 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
2listed device types
Class I 0Class II 2Class III 0
plus 6 registration records and 3 510(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
0active device licences
TWTaiwanTFDA
1valid device licences
Class I 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class I 2
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, 3 510(k), 0 PMA, 3 excluded
Saudi Arabia0 confirmed, 1 excluded
Manufacturer names merged into this page: SAN-M PACKAGE CO., LTD.

Company information

Country
Japan
City
Shimada-City Shizuoka

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

22016 · K160269
12022 · K221534

FDA listed device types

Mask, Surgical 1Respirator, Surgical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK221534Surgical Face Masks (Ear Loops And Tie-On)2022-09-16
USK160269Surgical Face Masks (Ear loops and Tie-on)2016-09-06
USK160271N95 Particulate Respirator and Surgical Mask, Models TN01-11 and TN01-122016-07-15

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