KIRLAND PERIODONTAL CURETTE 1102-RECPK13-13L

GUDID 00192896082304

KIRLAND PERIODONTAL CURETTE #13-13L DOUBLE ENDED BLADES LIGHT HANDLE

SONTEC INSTRUMENTS, INC.

Periodontal curette
Primary Device ID00192896082304
NIH Device Record Key962cec12-031e-4e7b-b5bb-7042816e6698
Commercial Distribution StatusIn Commercial Distribution
Brand NameKIRLAND PERIODONTAL CURETTE
Version Model Number1102-RECPK13-13L
Catalog Number1102-RECPK13-13L
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896082304 [Primary]

FDA Product Code

EMKCURETTE, SURGICAL, DENTAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896082304]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number8
Public Version Date2019-09-09
Device Publish Date2018-09-21

On-Brand Devices [KIRLAND PERIODONTAL CURETTE]

00192896082304KIRLAND PERIODONTAL CURETTE #13-13L DOUBLE ENDED BLADES LIGHT HANDLE
00192896050082KIRLAND PERIODONTAL CURETTE #13-13L DOUBLE ENDED BLADES STANDARD HANDLE

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