110038

GUDID 23596010033332

FEMORAL CANAL SUCTION ABSORBER LARGE 25MM DIAMETER

Smith & Nephew, Inc.

General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum General-purpose surgical suction system, vacuum
Primary Device ID23596010033332
NIH Device Record Key96d1e174-37ba-4de2-aeb3-0cd59cdc1713
Commercial Distribution StatusIn Commercial Distribution
Version Model Number110038
Catalog Number110038
Company DUNS109903521
Company NameSmith & Nephew, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
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
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
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
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
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
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
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
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
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS103596010033338 [Primary]
GS123596010033332 [Package]
Contains: 03596010033338
Package: BX [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JOLCATHETER AND TIP, SUCTION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-02-17
Device Publish Date2015-08-29

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00885556817667 - TULA2024-05-07 TULA KIT- UNILATERAL (NST007068)
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00885556890752 - ULTRABRACE2024-05-06 ULTRABRACE KIT
00885556890769 - FOOTPRINT2024-05-06 FOOTPRINT MINI PK 3.5MM
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