FDA.reportPublic FDA data

BD Kiestra B.V.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30101415913010141591BD Kiestra B.V.1N2026-01-01Marconilaan 6 Drachten Fryslan NL 9207 JC

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00382904449087BD Kiestra™ Methicillin-resistant Staphylococcus aureus (MRSA) Application - 444908+1(800)638-8663Technical_services@bd.com
00382904460921BD Kiestra™ T-junction - 446092+1(800)638-8663Technical_services@bd.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1461991452610934K222563BD Kiestra IdentifAQQV2023-08-31
1461991103217973K213280BD Kiestra Methicillin-resistant Staphylococcus aureus (MRSA) Application, BD Kiestra MRSA AppQQY2023-05-04
1461991471082541K191964BD Kiestra IdentifAQQV2021-11-03
1461991200129363
1461991272129705
1461991363948523
1461991620933544
1461991866419800
1461991904895491

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QQV22023-08-31
QQY12023-05-04

PMN#

GUDID#