Single Use Preloaded Sphincterotome V

GUDID 14953170403214

OLYMPUS MEDICAL SYSTEMS CORP.

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Primary Device ID14953170403214
NIH Device Record Key6f1e6a1f-0324-4222-9c37-1950bda9d9c3
Commercial Distribution StatusIn Commercial Distribution
Brand NameSingle Use Preloaded Sphincterotome V
Version Model NumberKD-V631M-07301A
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
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
GS104953170403217 [Primary]
GS114953170403214 [Package]
Contains: 04953170403217
Package: [1 Units]
In Commercial Distribution
GS154953170403212 [Package]
Package: [18 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KNSUnit, electrosurgical, endoscopic (with or without accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-21
Device Publish Date2018-01-05

On-Brand Devices [Single Use Preloaded Sphincterotome V]

14953170403238KD-V631M-07302A
14953170403221KD-V631M-07302S
14953170403214KD-V631M-07301A
14953170403207KD-V631M-07301S
14953170403191KD-V631M-07202A
14953170403184Single Use Preloaded Sphincterotome V
14953170403177KD-V631M-07201A
14953170403160KD-V631M-07201S
14953170403153KD-V611M-07302A
14953170403146KD-V611M-07302S
14953170403139KD-V611M-07301A
14953170403122KD-V611M-07301S
14953170403115KD-V611M-07252A
14953170403108KD-V611M-07252S
14953170403092KD-V611M-07251A
14953170403085KD-V611M-07251S
14953170403078KD-V611M-07202A
14953170403061KD-V611M-07202S
14953170403054KD-V611M-07201A
14953170403047KD-V611M-07201S
14953170345125KD-V631M-07302A
14953170345118KD-V631M-07302S
14953170345101KD-V631M-07301A
14953170345095KD-V631M-07301S
14953170345088KD-V631M-07202A
14953170345071Single Use Preloaded Sphincterotome V
14953170345064KD-V631M-07201A
14953170345057KD-V631M-07201S
14953170345040KD-V611M-07302A
14953170345033KD-V611M-07302S
14953170345026KD-V611M-07301A
14953170345019KD-V611M-07301S
14953170345002KD-V611M-07252A
14953170344999KD-V611M-07252S
14953170344982KD-V611M-07251A
14953170344975KD-V611M-07251S
14953170344968KD-V611M-07202A
14953170344951KD-V611M-07202S
14953170344944KD-V611M-07201A
14953170344937KD-V611M-07201S

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