Homemed solutions ltda

med solutions ltda

✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Saudi Arabia, Canada, South Korea, Israel — 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
11listed device types
Class I 8Class II 3Class III 0
plus 11 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
6registered devices
Class I 6
7 including historic records
SASaudi ArabiaSFDA
57registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
1 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
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 States11 registration records, 3 510(k), 0 PMA, 340 excluded
Brazil6 confirmed, 131 excluded
Saudi Arabia57 confirmed, 33 excluded
Canada0 confirmed, 48 excluded
Manufacturer names merged into this page: CMC MANUFACTURING LLC DBA CMC MED SOLUTIONS · SML MED-TECH SOLUTIONS LIMITED · med solutions ltda · Med-Tec Inc. bda CIVCO Medical Solutions and CIVCO Radiotherapy

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 510(k) clearances by year

12012 · K122201
12013 · K132084
12023 · K220884

FDA listed device types

showing 8 of 11
Adaptor, Bulbs, Miscellaneous, For Endoscope 1Accessories, Cleaning Brushes, For Endoscope 1Endoscopic Bite Block 1Needle, Aspiration And Injection, Disposable 1Basin For Endoscope Reprocessing 1Catheters, Suction, Tracheobronchial 1Tubeless Analysis, Gastric Acidity 1Dressing, Wound, Occlusive 1

Registration details (sample)

MarketIdentifierNameClass / date
USK220884Disposable Endoscope Valve Sets2023-01-17
USK132084PROTURA COUCH SOFTWARE2013-09-26
USK122201PROTURA COUCH SOFTWARE2012-08-30
BR82214240014GuardPro ValveClass I
BR82214240015Orion TrapClass I
BR82214240016GuardPro LinerClass I
SAME0000002101SFDAA00071Monarch™ Overhead Arm Positioner
SAME0000002101SFDAA00051Bra Extender

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