PHANEUF UTERINE ARTERY FORCEPS 525-459

GUDID 00192896045941

PHANEUF UTERINE ARTERY FORCEPS STRAIGHT JAW

SONTEC INSTRUMENTS, INC.

Open-surgery biopsy forceps, reusable Open-surgery biopsy forceps, reusable Open-surgery biopsy forceps, reusable
Primary Device ID00192896045941
NIH Device Record Keyb9c69bfe-1833-4d9c-b52b-84561344efe6
Commercial Distribution StatusIn Commercial Distribution
Brand NamePHANEUF UTERINE ARTERY FORCEPS
Version Model Number525-459
Catalog Number525-459
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

Device Dimensions

Length8.5 Inch
Length8.5 Inch
Length8.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896045941 [Primary]

FDA Product Code

HFBFORCEPS, BIOPSY, GYNECOLOGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896045941]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045941]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045941]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-07-12
Device Publish Date2018-09-14

On-Brand Devices [PHANEUF UTERINE ARTERY FORCEPS]

00192896045958PHANEUF UTERINE ARTERY FORCEPS ANGLED ON FLAT JAW
00192896045941PHANEUF UTERINE ARTERY FORCEPS STRAIGHT JAW

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