#10 – Micro Curette, Straight

GUDID 00840096203998

#10 – Micro Curette, Straight

KATALYST SURGICAL LLC

Bone curette, reusable
Primary Device ID00840096203998
NIH Device Record Key671b3a0c-4e44-4302-a01a-ac64b276011d
Commercial Distribution StatusIn Commercial Distribution
Brand Name#10 – Micro Curette, Straight
Version Model NumberN089-080
Company DUNS007883297
Company NameKATALYST SURGICAL LLC
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 Datefalse
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
GS100840096203998 [Primary]

FDA Product Code

FZSCurette, Surgical, General Use

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840096203998]

Moist Heat or Steam Sterilization


[00840096203998]

Moist Heat or Steam Sterilization


[00840096203998]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-19
Device Publish Date2020-05-11

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