Single Use Nasal Biliary Drainage Tube V

GUDID 14953170309479

OLYMPUS MEDICAL SYSTEMS CORP.

Biliary drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter Nasal biliary/pancreatic drainage catheter
Primary Device ID14953170309479
NIH Device Record Keyc8cc6b3e-7391-401f-98f1-3bb27cddebef
Commercial Distribution StatusIn Commercial Distribution
Brand NameSingle Use Nasal Biliary Drainage Tube V
Version Model NumberPBD-V812W-07
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170309472 [Primary]
GS114953170309479 [Package]
Contains: 04953170309472
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FGECATHETER, BILIARY, DIAGNOSTIC

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-21

On-Brand Devices [Single Use Nasal Biliary Drainage Tube V]

14953170309592PBD-V814W-07
14953170309578PBD-V814W-06
14953170309554PBD-V814W-05
14953170309530PBD-V813W-07
14953170309516PBD-V813W-06
14953170309493PBD-V813W-05
14953170309479PBD-V812W-07
14953170309455PBD-V812W-06
14953170309431PBD-V812W-05
14953170309417PBD-V811W-07
14953170309394PBD-V811W-06
14953170309370PBD-V811W-05
14953170309356PBD-V803W-07
14953170309332PBD-V803W-06
14953170309318PBD-V803W-05

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