INLET System Surgical Instrument

GUDID 08800089412495

Jeil Medical Corporation

Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable
Primary Device ID08800089412495
NIH Device Record Key7937c297-e244-43e8-b029-f8ea39a748ee
Commercial Distribution StatusIn Commercial Distribution
Brand NameINLET System Surgical Instrument
Version Model NumberIN111-078
Company DUNS688811603
Company NameJeil Medical Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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
GS108800089412495 [Primary]

FDA Product Code

FZXGuide, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


[08800089412495]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-24
Device Publish Date2021-11-16

On-Brand Devices [INLET System Surgical Instrument]

08800089411634IN111-181
08800089411627IN111-212
08800089411610IN111-175-L
08800089411603IN111-175-R
08800089411597IN112-122
08800089411511IN111-151
08800089411504IN111-ED-051
08800089411498IN113-HF-625
08800089411481IN113-HF-624
08800089411474IN111-038
08800089411467IN111-155
08800089411450IN112-107
08800089411443IN111-156
08800089411436IN24-JLST-008T
08800089411429IN24-HNST-012T
08800089411412IN24-HSST-008T
08800089411405IN24-HWST-012T
08800089411399IN24-LPST-004T
08800089411382IN24-SQST-004T
08800089411375IN24-STST-004T
08800089411368IN24-STST-008T
08800089411351IN24-XPST-008T
08800089411344IN111-149
08800089411337IN111-148
08800089411320IN111-150
08800089413744IN111-135
08800089413737IN111-010
08800089413720IN111-112
08800089413713IN111-113
08800089413706IN111-114
08800089413690IN111-115
08800089413683IN111-131
08800089413676IN111-132
08800089413669IN111-133
08800089413652IN112-23-703-L
08800089413645IN112-23-704
08800089413638IN112-28-701
08800089413621IN112-28-701-L
08800089413614IN112-121
08800089412525IN112-104
08800089412518IN114-008
08800089412501IN111-079
08800089412495IN111-078
08800089412488IN111-028
08800089412471IN111-047
08800089412464IN113-HF-103
08800089412457IN112-20-701-L
08800089412440IN111-125
08800089412433IN111-124
08800089412426IN111-027

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