Mod Kit Pulset™

GUDID 10709078003346

Mod Kit, Pulset 3cc Syringe 22g x 1" (.7 x 25mm) Safety 25u Balanced Heparin

WESTMED, INC.

Arterial blood sampling kit Arterial blood sampling kit

• Primary Device ID: 10709078003346
• NIH Device Record Key: fa13a117-4818-42d2-ba91-743b51f4efb9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mod Kit Pulset™
• Version Model Number: 3362-91
• 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078003349 [Primary]
GS1	10709078003346 [Package]; Contains: 00709078003349; 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: 3
• Public Version Date: 2019-06-25
• Device Publish Date: 2017-03-30

Devices Manufactured by WESTMED, INC.

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