PALMAZ GENESIS Transhepatic Biliary Stent on SLALOM .018" Delivery System PG1860BSS

GUDID 20705032038345

Shrt Gen on SL 18 X 60 BIL 80

CORDIS CORPORATION

Bare-metal biliary stent
Primary Device ID20705032038345
NIH Device Record Key2b18661e-60c8-49b9-83d3-ded098a10284
Commercial Distribution StatusIn Commercial Distribution
Brand NamePALMAZ GENESIS Transhepatic Biliary Stent on SLALOM .018" Delivery System
Version Model NumberPG1860BSS
Catalog NumberPG1860BSS
Company DUNS806136177
Company NameCORDIS CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110705032038348 [Primary]
GS120705032038345 [Package]
Contains: 10705032038348
Package: Box [1 Units]
In Commercial Distribution

FDA Product Code

FGEStents, drains and dilators for the biliary ducts

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-04
Device Publish Date2024-02-23

On-Brand Devices [PALMAZ GENESIS Transhepatic Biliary Stent on SLALOM .018" Delivery System]

20705032039397SDS Genesis 9x25mm 80 cm pro
20705032039069Shrt Gen on SL 24 X 60 BIL 80
20705032038826Shrt Gen on SL 24 X 40 BIL 80
20705032038345Shrt Gen on SL 18 X 60 BIL 80
20705032038185Shrt Gen on SL 18 X 50 BIL 80
20705032038024Shrt Gen on SL 18 X 40 BIL 80
20705032037300Shrt Gen on SL 15 X 40 BIL 80
20705032036938Shrt Gen on SL 12 X 60 BIL 135
20705032036921Shrt Gen on SL 12 X 60 BIL 80
20705032036785Shrt Gen on SL 12 X 50 BIL 80
20705032036648Shrt Gen on SL 12 X 40 BIL 80

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.