V.A.T.S BLACK SUTURE CUTTER

GUDID B09924059470

V.A.T.S BLACK SUTURE CUTTER

SONTEC INSTRUMENTS, INC.

Suture cutter, reusable Suture cutter, reusable Suture cutter, reusable
Primary Device IDB09924059470
NIH Device Record Key0000935c-a6ba-429c-b58c-551a8851426a
Commercial Distribution StatusIn Commercial Distribution
Brand NameV.A.T.S BLACK SUTURE CUTTER
Version Model Number2405-947
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

Length13 Inch
Length13 Inch
Length13 Inch
Length13 Inch
Length13 Inch
Length13 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896004467 [Primary]
HIBCCB09924059470 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09924059470]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09924059470]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09924059470]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-28
Device Publish Date2018-08-28

On-Brand Devices [V.A.T.S BLACK SUTURE CUTTER ]

B09924059490V.A.T.S BLACK SUTURE CUTTER
B09924059470V.A.T.S BLACK SUTURE CUTTER
B09924059450V.A.T.S BLACK SUTURE CUTTER

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