Bard Dulex Mesh 0120302

GUDID 00801741011900

Bard Dulex Mesh

Davol Inc.

Abdominal hernia surgical mesh, synthetic polymer, non-bioabsorbable Abdominal hernia surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

• Primary Device ID: 00801741011900
• NIH Device Record Key: 78b0c7d7-1a48-4abc-a8e7-39fa88952a7e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard Dulex Mesh
• Version Model Number: 0120302
• Catalog Number: 0120302
• Company DUNS: 001191048
• Company Name: Davol 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: 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: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com
• Phone: +1(800)562-0027
• Email: medical.services@crbard.com

Device Dimensions

• Length: 20 Centimeter
• Length: 20 Centimeter
• Length: 20 Centimeter
• Length: 20 Centimeter
• Length: 20 Centimeter
• Length: 20 Centimeter
• Width: 30 Centimeter
• Height: 2 Millimeter
• Length: 20 Centimeter
• Width: 30 Centimeter
• Height: 2 Millimeter
• Length: 20 Centimeter
• Width: 30 Centimeter
• Height: 2 Millimeter
• Length: 20 Centimeter
• Width: 30 Centimeter
• Height: 2 Millimeter
• Length: 20 Centimeter
• Width: 30 Centimeter
• Height: 2 Millimeter
• Length: 20 Centimeter
• Width: 30 Centimeter
• Height: 2 Millimeter
• Length: 20 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741011900 [Primary]

FDA Product Code

• FTL: Mesh, surgical, polymeric

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: 2018-11-08
• Device Publish Date: 2015-05-17

On-Brand Devices [Bard Dulex Mesh]

• 00801741011931: Bard Dulex Mesh
• 00801741011924: Bard Dulex Mesh
• 00801741011917: Bard Dulex Mesh
• 00801741011900: Bard Dulex Mesh
• 00801741011894: Bard Dulex Mesh
• 00801741011887: Bard Dulex Mesh
• 00801741011870: Bard Dulex Mesh
• 00801741011856: Bard Dulex Mesh
• 00801741011849: Bard Dulex Mesh
• 00801741011801: Bard Dulex Mesh
• 00801741011795: Bard Dulex Mesh
• 00801741011788: Bard Dulex Mesh