ENT Sinus 910-30110

GUDID 00817470011869

SERPENT STERILIZATION TRAY LID

Smith & Nephew, Inc.

Instrument tray
Primary Device ID00817470011869
NIH Device Record Keyd8cc08a1-6c1a-4b80-9609-5fbe3a7e6300
Commercial Distribution Discontinuation2018-08-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameENT Sinus
Version Model Number910-30110
Catalog Number910-30110
Company DUNS109903521
Company NameSmith & Nephew, 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)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100817470011869 [Primary]

FDA Product Code

MMOTRAY, SURGICAL, ENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00817470011869]

Moist Heat or Steam Sterilization


[00817470011869]

Moist Heat or Steam Sterilization


[00817470011869]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-08-09
Device Publish Date2015-08-29

On-Brand Devices [ENT Sinus]

00817470011869SERPENT STERILIZATION TRAY LID
00817470011845SERPENT STERILIZATION TRAY BASE
20817470009761MEDIENT MIDDLE TURBINATE IMPLANT 4-PACK
00817470009750MediENT Middle Turbinate Implant 1-pack
00817470009729VENTERA SINUS DILATION BALLOON 1-PACK
00817470006469ENTACT SEPTAL STAPLER 1-PACK
20817470006456ENTACT SEPTAL STAPLER 3-PACK
00885556724736SERPENT STERILIZATION TRAY LID

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