LIQUIFIX Precision Open

GUDID 05036912001458

ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer Surgical internal adhesive/sealant, synthetic polymer

• Primary Device ID: 05036912001458
• NIH Device Record Key: ce7423f0-49cc-4376-a485-1994d18bdb94
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIQUIFIX Precision Open
• Version Model Number: 72014033
• Company DUNS: 236059171
• Company Name: ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05036912001441 [Primary]
GS1	05036912001458 [Package]; Contains: 05036912001441; Package: Unit Carton [1 Units]; In Commercial Distribution
GS1	05036912001465 [Package]; Package: Shipper [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P220024

FDA Product Code

• PLJ: Tissue Adhesive Internal Use

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: 2023-07-03
• Device Publish Date: 2023-06-23

Devices Manufactured by ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

• 05036912001427 - LIQUIFIX FIX8: 2023-07-03
• 05036912001458 - LIQUIFIX Precision Open: 2023-07-03
• 05036912001458 - LIQUIFIX Precision Open: 2023-07-03
• 05036912000406 - LiquiBand Butyl: 2023-06-20
• 05036912001694 - LiquiBand Exceed: 2023-06-20
• 05036912001724 - LiquiBand Exceed XS: 2023-06-20
• 05036912001755 - LiquiBand Octyl Mini: 2023-06-20
• 05036912001519 - LiquiBand Secure: 2023-05-29
• 05036912001540 - LiquiBand Secure: 2023-05-29