THOMAS CURETTE 520-672

GUDID 00192896045866

THOMAS CURETTE MALLEABLE BLUNT TIPS SIZE 2

SONTEC INSTRUMENTS, INC.

General-purpose curette General-purpose curette General-purpose curette
Primary Device ID00192896045866
NIH Device Record Keydd6c55a8-cd23-4450-a539-98f7eb95d983
Commercial Distribution StatusIn Commercial Distribution
Brand NameTHOMAS CURETTE
Version Model Number520-672
Catalog Number520-672
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
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

Customer Support Contacts

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length11 Inch
Length11 Inch
Length11 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896045866 [Primary]

FDA Product Code

HCYCURETTE, UTERINE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896045866]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045866]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045866]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-09-10
Device Publish Date2018-09-14

On-Brand Devices [THOMAS CURETTE]

00192896045873THOMAS CURETTE MALLEABLE BLUNT TIPS SIZE 4
00192896045866THOMAS CURETTE MALLEABLE BLUNT TIPS SIZE 2
00192896045859THOMAS CURETTE MALLEABLE BLUNT TIPS SIZE 1

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