Bainbridge Forceps 115-600Q

GUDID 00192896116580

Bainbridge Forceps Delicate Longitudinal Serrations Straight Cross Serrated Tip Quantum

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID00192896116580
NIH Device Record Keyb1fc7524-7187-459c-aaec-439dbb8d598e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBainbridge Forceps
Version Model Number115-600Q
Catalog Number115-600Q
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 Latextrue
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

Device Dimensions

Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch
Length6 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896116580 [Primary]

FDA Product Code

HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

[00192896116580]

Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-02-28
Device Publish Date2024-02-20

On-Brand Devices [Bainbridge Forceps]

00192896075658BAINBRIDGE FORCEPS DELICATE CURVED LONGITUDINAL CROSS SERRATED TIP
00192896021280BAINBRIDGE FORCEPS DELICATE CURVED LONGITUDINAL SERRATIONS CROSS SERRATED TIP
00192896021273BAINBRIDGE FORCEPS DELICATE STRAIGHT LONGITUDINAL SERRATIONS CROSS SERRATED TIP
00192896021266BAINBRIDGE FORCEPS DELICATE CURVED LONGITUDINAL SERRATIONS CROSS SERRATED TIP
00192896021259BAINBRIDGE FORCEPS LONG PRECISE RIGHT ANGLED LONGITUDINAL SERRATIONS TIP
00192896021242BAINBRIDGE FORCEPS DELICATE STRAIGHT LONGITUDINAL SERRATIONS CROSS SERRATED TIP
00192896116580Bainbridge Forceps Delicate Longitudinal Serrations Straight Cross Serrated Tip Quantum
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