DUALX DUAL PORT CANNULA 50MM

GUDID B70712535588003US0

50MM US MANUFACTURE

AMPLIFY SURGICAL, INC.

Orthopaedic inorganic implant inserter/extractor, reusable

• Primary Device ID: B70712535588003US0
• NIH Device Record Key: a979da4c-1c6b-4e40-ac1a-b233007d862f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUALX DUAL PORT CANNULA 50MM
• Version Model Number: 12535588003US
• Company DUNS: 081021000
• Company Name: AMPLIFY SURGICAL, 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com
• Phone: 7652675439
• Email: udi@amplifysurgical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B70712535588003US0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181397

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

[B70712535588003US0]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-06
• Device Publish Date: 2025-05-29

On-Brand Devices [DUALX DUAL PORT CANNULA 50MM]

• B707125355800030: 50MM
• B70712535588003US0: 50MM US MANUFACTURE