DISSECTING FORCEPS INSERT

GUDID B09929012030

DISSECTING FORCEPS FENESTRATED DOUBLE-ACTION JAWS TUBE SHAFT

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable
Primary Device IDB09929012030
NIH Device Record Keya5e95368-2c59-47b2-be26-5ae2731494f5
Commercial Distribution StatusIn Commercial Distribution
Brand NameDISSECTING FORCEPS INSERT
Version Model Number2901-203
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

Length210 Millimeter
Length210 Millimeter
Length210 Millimeter
Length210 Millimeter
Length210 Millimeter
Length210 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896007482 [Primary]
HIBCCB09929012030 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09929012030]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09929012030]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09929012030]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-08
Device Publish Date2018-08-22

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