Neptune 2 0702020000

GUDID 37613154688280

4-Port Manifold

STRYKER CORPORATION

Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system Surgical fluid/smoke waste management system
Primary Device ID37613154688280
NIH Device Record Keye522d440-14c1-445e-8946-ce06fe47a58c
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeptune 2
Version Model Number0702020000
Catalog Number0702020000
Company DUNS196548481
Company NameSTRYKER CORPORATION
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 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)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 Identifiers

Device Issuing AgencyDevice ID
GS107613154688289 [Primary]
GS137613154688280 [Package]
Contains: 07613154688289
Package: pack [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JCXAPPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-20
Device Publish Date2016-09-23

On-Brand Devices [Neptune 2]

37613154733225Specimen Collection 4-Port Manifold
37613154688297Single Port Manifold
376131546882804-Port Manifold

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