DAVIS GALLSTONE SCOOP 1100-521L

GUDID 00192896081543

DAVIS GALLSTONE SCOOP DOUBLE ENDED BLUNT TIPS

SONTEC INSTRUMENTS, INC.

Urethral dilator, reusable
Primary Device ID00192896081543
NIH Device Record Keybd129867-88d4-40d2-9cd8-f47cdf206867
Commercial Distribution StatusIn Commercial Distribution
Brand NameDAVIS GALLSTONE SCOOP
Version Model Number1100-521L
Catalog Number1100-521L
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
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
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

Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896081543 [Primary]

FDA Product Code

FHLSCOOP

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896081543]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-02-06
Device Publish Date2018-09-20

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