HEARTLINE GEMINI DISSECTING FORCEPS

GUDID B09928007828S0

HEARTLINE GEMINI DISSECTING FORCEPS SPREADING JAW

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Primary Device IDB09928007828S0
NIH Device Record Keyf4f11960-0765-4453-b7fb-04b9af2d9c9d
Commercial Distribution Discontinuation2018-06-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameHEARTLINE GEMINI DISSECTING FORCEPS
Version Model Number2800-7828S
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

Length20.3 Centimeter
Device Size Text, specify0
Length20.3 Centimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB09928007828S0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09928007828S0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B09928007828S0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2018-07-06
Device Publish Date2016-08-19

On-Brand Devices [HEARTLINE GEMINI DISSECTING FORCEPS]

B099280078280HEARTLINE GEMINI DISSECTING FORCEPS SPREADING JAW
B09928007828S0HEARTLINE GEMINI DISSECTING FORCEPS SPREADING JAW
B09928007828L0HEARTLINE GEMINI DISSECTING FORCEPS SPREADING JAW

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