Pulset™ 3CC Syringe, 22G X 1"

GUDID 00709078003233

Pulset™ 3CC Syringe 22G X 1", Safety Tip, 25U BH

WESTMED, INC.

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• Primary Device ID: 00709078003233
• NIH Device Record Key: 73699ad8-a2bb-4127-ae6a-9cdcbf2da2a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pulset™ 3CC Syringe, 22G X 1"
• Version Model Number: 3302-91
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 100
• 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: false
• 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	00709078003233 [Primary]
GS1	00709078003240 [Unit of Use]
GS1	10709078003247 [Unit of Use]

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: 2017-03-20

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