HomeCanadaGERMIPHENE CORPORATION

GERMIPHENE CORPORATION

Canada · Brantford
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Australia, Russia — 4 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
3listed device types
Class I 3Class II 0Class III 0
plus 3 registration records and 5 510(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
2active device licences
Class II 2
3 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class I 1IIb 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2a 1
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 States3 registration records, 5 510(k), 0 PMA
Canada2 confirmed, 0 excluded
Manufacturer names merged into this page: GERMIPHENE CORP. · GERMIPHENE CORPORATION

Company information

Country
Canada
City
Brantford

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

11989 · K894933
11994 · K942851
21997 · K961289
11998 · K983847

FDA listed device types

Cleaner, Ultrasonic, Medical Instrument 1Disinfectant, Medical Devices 1Detergent 1

Registration details (sample)

MarketIdentifierNameClass / date
USK983847MODIFICATION OF: ODYSSEY I DENTAL WATER UNIT1998-12-01
USK961289VAPOPHENE1997-12-04
USK964796ODYSSEY I DENTAL WATER UNIT1997-05-14
CA74874MAXTER LATEX EXAMINATION GLOVESClass II
CA81204CAREPLUS NON STERILE AMBIDEXTROUS SINGLE USE LATEX GLOVESClass II

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