COOLEY PERIPHERAL VASCULAR CLAMP

GUDID B09921002500

COOLEY PERIPHERAL VASCULAR CLAMP ANGLED JAW ANGLED SHANK

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device IDB09921002500
NIH Device Record Key5eec695f-de37-4535-a4e9-340a4a16e618
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOOLEY PERIPHERAL VASCULAR CLAMP
Version Model Number2100-250
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

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

Device Dimensions

Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896010192 [Primary]
HIBCCB09921002500 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09921002500]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09921002500]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09921002500]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-08-21
Device Publish Date2018-08-24

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