Aspira Valve Repair Kit 4992306

GUDID 10801741045056

Aspira Valve Repair Kit

Bard Access Systems, Inc.

Pleural/peritoneal drainage catheterization kit Pleural/peritoneal drainage catheterization kit

• Primary Device ID: 10801741045056
• NIH Device Record Key: 441f7e5f-d624-49ba-b017-7fd7ea39ddc3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aspira Valve Repair Kit
• Version Model Number: 4992306
• Catalog Number: 4992306
• Company DUNS: 044611812
• Company Name: Bard Access Systems, Inc.
• 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: 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)545-0890
• Email: medical.services@crbard.com
• Phone: +1(800)545-0890
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741045059 [Primary]
GS1	10801741045056 [Package]; Contains: 00801741045059; Package: CA [5 Units]; In Commercial Distribution
GS1	20801741045053 [Package]; Package: BX [60 Units]; In Commercial Distribution

FDA Product Code

• FJS: CATHETER, PERITONEAL, LONG-TERM INDWELLING

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: 2015-11-20

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