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Delcon

✓ Record-verifiedregistrations found in 3 marketsEU SRN IT-MF-000014234

This company has registrations in European Union, United States, Israel — 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
66UDI-DI device records
Class I 47IVD A 19
USUnited StatesFDA openFDA
3listed device types
Class I 2Class II 1Class III 0
plus 6 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
0registered device records
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
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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.

European Union66 raw hits, 0 excluded, 66 confirmed
United States6 registration records, 0 510(k), 0 PMA
Brazil0 confirmed, 1 excluded
Saudi Arabia0 confirmed, 2 excluded
Manufacturer names merged into this page: DELCON SRL

Regulatory identity

EU manufacturer SRN
IT-MF-000014234
Exhibition record
CMEF 87th (Spring 2023, Shanghai)

Company information

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

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

Registration details (sample)

MarketIdentifierNameClass / date
EU08033928530856Milano GULF COAST - Basic versionClass I
EU08033928530849Milano GULF COAST - RFID versionClass I
EU08033928530832Milano VERSITI - Basic versionClass I
EU08033928530825Milano VERSITI - RFID versionClass I

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