COOLEY MULTI-PURPOSE CLAMP

GUDID B09921002200

COOLEY MULTI PURPOSE CLAMP ANGLED

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device IDB09921002200
NIH Device Record Key351eadd5-646b-4b8e-9c73-c552623b58e6
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOOLEY MULTI-PURPOSE CLAMP
Version Model Number2100-220
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 Usetrue
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

Phone303-790-9411
Emailinfo@sontecinstruments.com
Phone303-790-9411
Emailinfo@sontecinstruments.com
Phone303-790-9411
Emailinfo@sontecinstruments.com

Device Dimensions

Length9.75 Inch
Length9.75 Inch
Length9.75 Inch
Length9.75 Inch
Length9.75 Inch
Length9.75 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896010161 [Primary]
HIBCCB09921002200 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[B09921002200]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09921002200]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09921002200]

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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