FDA.reportPublic FDA data

POIESIS MEDICAL, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30094250083009425008POIESIS MEDICAL, LLC1Y2020-04-25151 Fern Street Suite 1 JUPITER FL US 33458

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
10852732004002Duette™ - 18FR Duettte™Indwelling Urinary Catheter+1(877)487-5740sales@poiesismedical.com
10852732004019Duette™ - 18FR Duette™ Indwelling Urinary Catheter Tray+1(877)487-5740sales@poiesismedical.com
10852732004026Duette™ - 16FR Duette™ Indwelling Urinary Catheter+1(877)487-5740sales@poiesismedical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1425131858036352K941488DEVMED DOUBLE-BALLOON UROLOGICAL CATHETEREZL1994-11-30

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EZL11994-11-30

PMN#

GUDID#