POWER PULSE 104834

GUDID 00616258005102

PPS ANCILLARY PACK, FG PKG

Bayer Healthcare LLC

General-purpose catheter connector, sterile General-purpose catheter connector, sterile

• Primary Device ID: 00616258005102
• NIH Device Record Key: 86f6e267-33f1-4e82-83f7-cc67cb9a25eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POWER PULSE
• Version Model Number: 104834-002
• Catalog Number: 104834
• Company DUNS: 079415074
• Company Name: Bayer Healthcare LLC
• 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: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 763-780-4555
• Email: michael.burnside@bayer.com
• Phone: 763-780-4555
• Email: michael.burnside@bayer.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616258005102 [Primary]
GS1	10616258005109 [Package]; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• KRA: Catheter, Continuous Flush

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: 2018-08-09
• Device Publish Date: 2014-10-09

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