SonoSurg Long Curved Scissors 5mm O.D, HF, Pistol

GUDID 14953170208598

OLYMPUS MEDICAL SYSTEMS CORP.

Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable Soft-tissue ultrasonic surgical system holder/tip, reusable
Primary Device ID14953170208598
NIH Device Record Key650a8089-b7ff-49fd-8d53-282b1b57d5a3
Commercial Distribution StatusIn Commercial Distribution
Brand NameSonoSurg Long Curved Scissors 5mm O.D, HF, Pistol
Version Model NumberT3105
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170208591 [Primary]
GS114953170208598 [Package]
Contains: 04953170208591
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LFLInstrument, ultrasonic surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


[14953170208598]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2018-10-08
Device Publish Date2017-10-06

Devices Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

04953170452932 - TRACHEAL INTUBATION FIBERSCOPE2024-04-22
14953170460064 - Single Use Biliary Drainage Stent V2024-04-02
14953170460088 - Single Use Biliary Drainage Stent V2024-04-02
14953170460101 - Single Use Biliary Drainage Stent V2024-04-02
14953170460132 - Single Use Biliary Drainage Stent V2024-04-02
14953170460330 - Single Use Biliary Drainage Stent V2024-04-02
14953170460378 - Single Use Biliary Drainage Stent V2024-04-02
14953170460613 - Single Use Biliary Drainage Stent V2024-04-02

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