Suction Adapter 0034850

GUDID 10801741049245

ReliaVac Auxiliary Suction Adapter

C. R. Bard, Inc.

Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connector Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set Closed-wound drain connection tubing set

• Primary Device ID: 10801741049245
• NIH Device Record Key: b22f8621-6bd1-4a29-8b40-95eb31e2cc66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suction Adapter
• Version Model Number: 0034850
• Catalog Number: 0034850
• Company DUNS: 016898496
• Company Name: C. R. Bard, 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: 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

Customer Support Contacts

• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741049248 [Primary]
GS1	10801741049245 [Package]; Contains: 00801741049248; Package: CA [10 Units]; In Commercial Distribution

FDA Product Code

• GCY: APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-30
• Device Publish Date: 2020-09-22

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