0215114000

GUDID 34546540865114

Trocar

STRYKER CORPORATION

Whole-blood-recovery autotransfusion system, powered Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable
Primary Device ID34546540865114
NIH Device Record Key89a1f0c3-6513-47ab-9750-31eeed229e8f
Commercial Distribution StatusIn Commercial Distribution
Version Model Number0215114000
Catalog Number0215114000
Company DUNS196548481
Company NameSTRYKER CORPORATION
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 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)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104546540865113 [Primary]
GS134546540865114 [Package]
Contains: 04546540865113
Package: pack [10 Units]
In Commercial Distribution

FDA Product Code

GCYAPPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-25
Device Publish Date2018-09-24

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07613327627701 - KNOTILUS+2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
07613327623796 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HIP
07613327623833 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP
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07613327634693 - Iconix2024-03-12
07613327616675 - SPY2024-03-06
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