0215-089-000

GUDID 34546540865053

Bilateral Evacuator Tube Set

STRYKER CORPORATION

Whole-blood-recovery autotransfusion system, powered
Primary Device ID34546540865053
NIH Device Record Keyd853abd1-0c3d-46b9-bb9c-25543e22552d
Commercial Distribution Discontinuation2019-03-31
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number0215089000
Catalog Number0215-089-000
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540865052 [Primary]
GS134546540865053 [Package]
Contains: 04546540865052
Package: pack [10 Units]
Discontinued: 2019-03-31
Not 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 StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-19
Device Publish Date2018-09-24

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