#11 – Micro Curette, Angled

GUDID 00840096204001

#11 – Micro Curette, Angled

KATALYST SURGICAL LLC

Bone curette, reusable
Primary Device ID00840096204001
NIH Device Record Key43c0b762-4ba6-45a5-8aa8-94308daf6229
Commercial Distribution StatusIn Commercial Distribution
Brand Name#11 – Micro Curette, Angled
Version Model NumberN090-080
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
GS100840096204001 [Primary]

FDA Product Code

FZSCurette, Surgical, General Use

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840096204001]

Moist Heat or Steam Sterilization


[00840096204001]

Moist Heat or Steam Sterilization


[00840096204001]

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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