CAROTID CLAMP

GUDID B09921003780

CAROTID CLAMP ATRAUMATIC JAW

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device IDB09921003780
NIH Device Record Key2251144d-a010-482d-94d7-d9c8fdb69d56
Commercial Distribution Discontinuation2018-06-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCAROTID CLAMP
Version Model Number2100-378
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 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

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

Device Dimensions

Length7 Inch
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB09921003780 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09921003780]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B09921003780]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2018-07-06
Device Publish Date2017-08-08

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