Home›USA›BD MEDICAL

BD MEDICAL

USA · Holdrege

✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Canada, Taiwan — 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

8listed device types

Class I 1Class II 7Class III 0

plus 11 registration records and 3 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

1registered devices

Class II 1

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

5active device licences

Class II 5

9 including historic records

TWTaiwanTFDA

1valid device licences

Class II 1

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 States11 registration records, 3 510(k), 0 PMA, 33 excluded

Brazil1 confirmed, 5 excluded

Canada5 confirmed, 3 excluded

Manufacturer names merged into this page: BD MEDICAL · BD MEDICAL DEVELOPMENT · BD MEDICAL - PHARMACEUTICAL SYSTEMS

FDA 510(k) clearances by year

12001 · K010188

12011 · K112434

12012 · K120384

FDA listed device types

Tube, Tracheostomy (W/Wo Connector) 1Piston Syringe With Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact 1Syringe, Piston 1Syringe, Antistick 1Tube, Tracheal (W/Wo Connector) 1Implant, Absorbable, (Scleral Buckling Methods) 1Cuff, Tracheal Tube, Inflatable 1Brush, Scrub, Operating-Room 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K120384	PROTECTOR, INJECTOR, CONNECTOR	2012-09-12
US	K112434	BD ORAL/ENTERAL SYRINGE WITH BD UNIVIA CONNECTION	2011-09-29
US	K010188	BD ECLIPSE HYPODERMIC NEEDLE	2001-03-01
BR	10033430526	CANETA APLICADORA	Class II
CA	2721	B-D AUTO-INJECTOR	Class II
CA	14722	HYPOINT NEEDLES	Class II
CA	63971	BD SAFETY-LOK INFUSION SET WITH FILTER	Class II

BD MEDICAL

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

Similar companies