Neptune 2 0702-020-001

GUDID 37613154733225

Specimen Collection 4-Port Manifold

STRYKER CORPORATION

Surgical fluid/smoke waste management system

• Primary Device ID: 37613154733225
• NIH Device Record Key: f76fff3f-fa2d-4c26-856c-88116126ab09
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neptune 2
• Version Model Number: 0702020001
• Catalog Number: 0702-020-001
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613154733224 [Primary]
GS1	37613154733225 [Package]; Contains: 07613154733224; Package: pack [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132671

FDA Product Code

• JCX: APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-01-20
• Device Publish Date: 2016-09-23

On-Brand Devices [Neptune 2]

• 37613154733225: Specimen Collection 4-Port Manifold
• 37613154688297: Single Port Manifold
• 37613154688280: 4-Port Manifold