HEARTLINE BIOPSY GRASPING FORCEPS

GUDID B09928003750

HEARTLINE BIOPSY GRASPING FORCEPS

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Primary Device IDB09928003750
NIH Device Record Key0f92d65e-81a7-4be5-819c-78b59c2997c2
Commercial Distribution Discontinuation2018-06-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameHEARTLINE BIOPSY GRASPING FORCEPS
Version Model Number2800-375
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

Device Dimensions

Length23.5 Centimeter
Device Size Text, specify0
Length23.5 Centimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB09928003750 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09928003750]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B09928003750]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number7
Public Version Date2018-07-06
Device Publish Date2016-08-19

On-Brand Devices [HEARTLINE BIOPSY GRASPING FORCEPS]

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

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