HAYES INTESTINAL CLAMP 10-0567

GUDID 00192896072091

HAYES INTESTINAL CLAMP ATRAUMATIC JAW

SONTEC INSTRUMENTS, INC.

Pylorus separator
Primary Device ID00192896072091
NIH Device Record Keyb1970427-d7de-4be8-882f-93f1e0acc134
Commercial Distribution StatusIn Commercial Distribution
Brand NameHAYES INTESTINAL CLAMP
Version Model Number10-0567
Catalog Number10-0567
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

Device Dimensions

Length12.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896072091 [Primary]

FDA Product Code

FFRDEVICE, LOCKING, FOR INTESTINAL CLAMP

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896072091]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-15
Device Publish Date2018-09-19

On-Brand Devices [HAYES INTESTINAL CLAMP]

00192896072091HAYES INTESTINAL CLAMP ATRAUMATIC JAW
00192896011526HAYES INTESTINAL CLAMP ANGLED TIP

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