HEMORRHOIDAL SUCTION LIGATOR

GUDID B0995085750

HEMORRHOIDAL SUCTION LIGATOR WITH LOADING CONE UP ANGLED

SONTEC INSTRUMENTS, INC.

Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator
Primary Device IDB0995085750
NIH Device Record Key9fd04288-b438-47eb-baf2-45907ca390fc
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEMORRHOIDAL SUCTION LIGATOR
Version Model Number508-575
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length7.75 Inch
Length7.75 Inch
Length7.75 Inch
Length7.75 Inch
Length7.75 Inch
Length7.75 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896044784 [Primary]
HIBCCB0995085750 [Previous]

FDA Product Code

FHNLigator, Hemorrhoidal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B0995085750]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B0995085750]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B0995085750]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-08
Device Publish Date2018-09-06

On-Brand Devices [HEMORRHOIDAL SUCTION LIGATOR]

B0995085800HEMORRHOIDAL SUCTION LIGATOR WITH LOADING CONE DOWN ANGLED
B0995085750HEMORRHOIDAL SUCTION LIGATOR WITH LOADING CONE UP ANGLED

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.