BOEHRINGER® CareConnect™ External Female Catheter Regulator 7620

GUDID 70816286020897

CareConnect™ External Female Catheter Regulator

BOEHRINGER LABORATORIES, LLC

Vacuum suction regulator/regulation set, general-purpose

• Primary Device ID: 70816286020897
• NIH Device Record Key: 5988faf8-9ed9-4474-94b1-a1786dbd8945
• Commercial Distribution Discontinuation: 2019-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BOEHRINGER® CareConnect™ External Female Catheter Regulator
• Version Model Number: 7620
• Catalog Number: 7620
• Company DUNS: 079991657
• Company Name: BOEHRINGER LABORATORIES, LLC
• 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: false
• 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: 610-278-0900
• Email: info@boehringerlabs.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10816286020895 [Primary]
GS1	70816286020897 [Package]; Contains: 10816286020895; Package: Box [10 Units]; Not in Commercial Distribution

FDA Product Code

• KDP: Regulator, Vacuum

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-12
• Device Publish Date: 2019-06-01

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