HomeTürkiyeBIMED TEKNIK ALETLER SANAYI TICARET AS

BIMED TEKNIK ALETLER SANAYI TICARET AS

Türkiye · Beylikduzu ?Stanbul
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 2 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
1listed device types
Class I 0Class II 1Class III 0
plus 1 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
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
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 States1 registration records, 1 510(k), 0 PMA, 1 excluded
Brazil2 confirmed, 0 excluded
Manufacturer names merged into this page: Bimed Teknik Aletler Sanayi & Ticaret A.S. · BIMED TEKNIK ALETLER SANAYI TICARET AS

Company information

Country
Türkiye
City
Beylikduzu ?Stanbul

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

12025 · K250733

FDA listed device types

Syringe, Piston 1

Registration details (sample)

MarketIdentifierNameClass / date
USK2507333DOSE 1ml Syringe2025-07-03
BR80451960111NPH MEDICAL SERINGA DESCARTÁVEL SEM AGULHAClass II
BR80451960099NPH MEDICAL SERINGA DESCARTÁVEL COM AGULHAClass II

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