TROUSSEAU TRACHEAL DILATOR RETRACTOR 502-384

GUDID 00192896044197

TROUSSEAU TRACHEAL DILATOR RETRACTOR ADULT LARGE SHAFT

SONTEC INSTRUMENTS, INC.

Tracheal surgery dilator, reusable
Primary Device ID00192896044197
NIH Device Record Key85ae0bd5-e83c-4d93-bcc6-ec4fe1c1992a
Commercial Distribution StatusIn Commercial Distribution
Brand NameTROUSSEAU TRACHEAL DILATOR RETRACTOR
Version Model Number502-384
Catalog Number502-384
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

Length5.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896044197 [Primary]

FDA Product Code

KCGDILATOR, TRACHEAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896044197]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-11-22
Device Publish Date2018-09-14

On-Brand Devices [TROUSSEAU TRACHEAL DILATOR RETRACTOR]

00192896044197TROUSSEAU TRACHEAL DILATOR RETRACTOR ADULT LARGE SHAFT
00192896044180TROUSSEAU TRACHEAL DILATOR RETRACTOR PEDIATRIC SMALL SHAFT
00192896044173TROUSSEAU TRACHEAL DILATOR RETRACTOR ADOLESCENT MEDIUM SHAFT

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.