TITANIUM DEBAKEY AORTA CLAMP

GUDID B09926002040

TITANIUM DEBAKEY MORRIS AORTA CLAMP

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device IDB09926002040
NIH Device Record Key79ceaeda-eaa4-4d84-9574-231f5bbc8b61
Commercial Distribution Discontinuation2018-06-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameTITANIUM DEBAKEY AORTA CLAMP
Version Model Number2600-204
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
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

Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM

Device Dimensions

Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB09926002040 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09926002040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B09926002040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2018-07-06
Device Publish Date2017-08-08

On-Brand Devices [TITANIUM DEBAKEY AORTA CLAMP]

B09926002040TITANIUM DEBAKEY MORRIS AORTA CLAMP
B09926002020TITANIUM DEBAKEY MORRIS AORTA CLAMP
B09926002000TITANIUM DEBAKEY MORRIS AORTA CLAMP

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