Surgical Instrument

GUDID 08800089404032

Jeil Medical Corporation

Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable
Primary Device ID08800089404032
NIH Device Record Keyaa39522e-39b6-47b0-99cd-f8315695c00b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurgical Instrument
Version Model Number112-156
Company DUNS688811603
Company NameJeil Medical Corporation
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800089404032 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


[08800089404032]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-08
Device Publish Date2022-08-31

On-Brand Devices [Surgical Instrument]

08806390878807112-081(M)
08806390878791111-010(M)
08806390878784112-060(M)
08809282819957111-083-L
08809282819940111-083-R
08809282819933111-082-L
08809282819926111-082-R
08806390879101112-129
08806390876285111-230-R
08806390876278111-230-L
08806390876261111-229-R
08806390876254111-229-L
08806390876247111-228-R
08806390876230111-228-L
08806390876223111-227-R
08806390876216111-227-L
08806390876209111-226
08806390801423111-095-R
08806390801416111-095-L
08809282815690112-074
08806390822633910.14AS01
08806390850759112-120
08806390883733112-129-7
08806390883726112-129-6
08806390883719112-129-5
08806390877831112-129-4
08806390877824112-129-3
08806390884006LS-420
08809282819841112-087
08806390874298111-206
08806390810326114-009
08806390810302114-007
08809282819902111-089
08809282819872111-085
08809282819865111-084
08809282818813111-087
08809282818806111-086
08809282818745111-080
08809282815591111-060
08809282815584111-059
08809282815577111-058
08809282815560111-057
08809282815553111-056
08809282815546111-055
08809282815492111-068-4
08809282815485111-068-3
08809282815478111-068-2
08809282815461111-068-1
08809282811722111-047
08809282811715111-046

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