HEARTLINE BIOPSY GRASPING FORCEPS

GUDID B0992800375S0

HEARTLINE BIOPSY GRASPING FORCEPS

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable
Primary Device IDB0992800375S0
NIH Device Record Key7d97b484-be8e-4e05-90d1-8e510d32b012
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEARTLINE BIOPSY GRASPING FORCEPS
Version Model Number2800-375S
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
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length17 Centimeter
Length17 Centimeter
Length17 Centimeter
Length17 Centimeter
Length17 Centimeter
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter
Device Size Text, specify0
Length17 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896010888 [Primary]
HIBCCB0992800375S0 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0992800375S0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-24
Device Publish Date2018-08-24

On-Brand Devices [HEARTLINE BIOPSY GRASPING FORCEPS]

B0992800375S0HEARTLINE BIOPSY GRASPING FORCEPS
B0992800375L0HEARTLINE BIOPSY GRASPING FORCEPS
B09928003750HEARTLINE BIOPSY GRASPING FORCEPS

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