Lid

GUDID 00851599007532

JACE MEDICAL, LLC

Sterilization/disinfection container 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 ID00851599007532
NIH Device Record Key84aa15eb-9942-4ba7-a0b6-3b72f617a4bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameLid
Version Model Number301.010.10
Company DUNS063554875
Company NameJACE MEDICAL, LLC
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100851599007532 [Primary]

FDA Product Code

JDQCerclage, Fixation

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


[00851599007532]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-09-10
Device Publish Date2016-08-15

On-Brand Devices [Lid]

00851599007532301.010.10
00851599007273315.010.20

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