Single Use Cannula V

GUDID 14953170183833

Single Use Cannula V

OLYMPUS MEDICAL SYSTEMS CORP.

Cholangiopancreatography catheter, single-use
Primary Device ID14953170183833
NIH Device Record Key505bc213-b40e-4f22-bd18-4834c0a0d281
Commercial Distribution StatusIn Commercial Distribution
Brand NameSingle Use Cannula V
Version Model NumberPR-V435Q
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170183836 [Primary]
GS114953170183833 [Package]
Contains: 04953170183836
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ODDEndoscopic retrograde cholangiopancreatography (ERCP) cannula

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 Cannula V]

14953170183833Single Use Cannula V
14953170183819PR-V434Q
14953170183796Single Use Cannula V
14953170183772Single Use Cannula V
14953170183758Single Use Cannula V
14953170183734PR-V416Q
14953170183710Single Use Cannula V
14953170183697Single Use Cannula V
14953170183635PR-V227Q
14953170183611PR-V220Q
14953170183574PR-V216Q
14953170183550PR-V214Q

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