HomeFranceMACO PHARMA

MACO PHARMA

France · Mouvaux Hauts-De
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Australia, Hong Kong, Israel, Russia — 6 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 2Class II 2Class III 0
plus 6 registration records and 0 510(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
7active device licences
Class II 6Class IV 1
13 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
16active ARTG entries
Class I 2Class III 1IIa 1IIb 11Class Is (sterile) 1
HKHong KongMDACS
3valid listings
Class III 3
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
8active registrations
Class 2a 5Class 2b 3
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, 0 510(k), 0 PMA, 1 excluded
Canada7 confirmed, 0 excluded
Manufacturer names merged into this page: MACO PHARMA · MACOPHARMA

Company information

Country
France
City
Mouvaux Hauts-De

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 listed device types

Device, Mixing And Weighing, Semi-Automated 1Microfilter, Blood Transfusion 1Supplies, Blood-Bank 1Device, Heat-Sealing 1

Registration details (sample)

MarketIdentifierNameClass / date
CA61264POCHES ALUMINIUM POUR CONGELATIONClass II
CA61265SOLUTION DE CONSERVATION DES PLAQUETTESClass II
CA69160SYSTEME THERAFLEX-MB PLASMAClass IV

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