FDA.reportPublic FDA data

CORTEC GMBH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30147666353014766635CORTEC GMBH1N2020-04-25Neuer Messplatz 3 Freiburg i. Br. Baden-Wurttemberg DE 79108

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
04260656590003AirRay® Electrode Connection Cable US - Connector Block 8 Channel+4976170888100support@cortec-neuro.com
04260656590034AirRay® Electrode Connection Cable US - Connector Block 32 Channel+4976170888100support@cortec-neuro.com
04260656590041AirRay® Electrode Connection Cable US - Patient Cable 8 Channel+4976170888100support@cortec-neuro.com
04260656590072AirRay® Electrode Connection Cable US - Patient Cable 32 Channel+4976170888100support@cortec-neuro.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2290451695934297K183437AirRay Subdural Cortical ElectrodesGYC2019-03-12

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GYC12019-03-12

PMN#

GUDID#