Pulset™

GUDID 10709078005104

Modified Kit, Pulset™ 1cc syringe 25g x 5/8" Safety Tip™ ~25u balanced heparin

WESTMED, INC.

Arterial blood sampling kit

• Primary Device ID: 10709078005104
• NIH Device Record Key: 65b5cc18-13e8-48bc-af56-68bd33f19c56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pulset™
• Version Model Number: 3165-91
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078005107 [Primary]
GS1	10709078005104 [Package]; Contains: 00709078005107; Package: [100 Units]; In Commercial Distribution

FDA Product Code

• CBT: Arterial Blood Sampling Kit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-22

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