STERNAL WIRE TWISTER NEEDLE HOLDER 1103-152Q

GUDID 00192896051768

STERNAL WIRE TWISTER NEEDLE HOLDER TUNGSTEN CARBIDE TIP

SONTEC INSTRUMENTS, INC.

Needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable Suturing needle holder, reusable
Primary Device ID00192896051768
NIH Device Record Keydfb34e38-96c3-406d-8a4f-a2352bad0552
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTERNAL WIRE TWISTER NEEDLE HOLDER
Version Model Number1103-152Q
Catalog Number1103-152Q
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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
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

Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896051768 [Primary]

FDA Product Code

HXKHOLDER, NEEDLE; ORTHOPEDIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896051768]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-09-18
Device Publish Date2018-09-24

On-Brand Devices [STERNAL WIRE TWISTER NEEDLE HOLDER]

00192896082656STERNAL WIRE TWISTER NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED BROAD TIP
00192896051782STERNAL WIRE TWISTER NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED BROAD TIP
00192896051775STERNAL WIRE TWISTER NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED BROAD TIP
00192896051768STERNAL WIRE TWISTER NEEDLE HOLDER TUNGSTEN CARBIDE TIP
00192896051744STERNAL WIRE TWISTER NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED BROAD TIP
00192896105676Sternal Wire Twister Needle Holder Tungsten Carbide Serrated Broad 5 X 20 Millimeter Jaw
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.