MICASEPT ANATOMICAL DRESSING FORCEPS 20919-90

GUDID 00192896092082

MICASEPT ANATOMICAL DRESSING FORCEPS WITHOUT RATCHET CURVED DOWN TIP SIDE OPENING

SONTEC INSTRUMENTS, INC.

Rigid endoscopic grasping forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable
Primary Device ID00192896092082
NIH Device Record Keyd07ef282-dce8-4081-82fa-47677550616b
Commercial Distribution StatusIn Commercial Distribution
Brand NameMICASEPT ANATOMICAL DRESSING FORCEPS
Version Model Number20919-90
Catalog Number20919-90
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

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896092082 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896092082]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-24
Device Publish Date2018-11-22

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