LiquiBand Butyl

GUDID 05036912000406

ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

Skin-approximation adhesive

• Primary Device ID: 05036912000406
• NIH Device Record Key: 4f629395-f862-4bac-b749-91b486610e0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiquiBand Butyl
• Version Model Number: LQB001
• Company DUNS: 236059171
• Company Name: ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED
• 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: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com
• Phone: +448444125754
• Email: Info@LiquiBand.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05036912000406 [Package]; Contains: 05036912000758; Package: Carton [12 Units]; In Commercial Distribution
GS1	05036912000758 [Primary]
GS1	05036912000987 [Package]; Package: Shipper Carton [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122446

FDA Product Code

• MPN: Tissue Adhesive For The Topical Approximation Of Skin

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: 2023-06-20
• Device Publish Date: 2023-06-12

Devices Manufactured by ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

• 05036912001427 - LIQUIFIX FIX8: 2023-07-03
• 05036912001458 - LIQUIFIX Precision Open: 2023-07-03
• 05036912000406 - LiquiBand Butyl: 2023-06-20
• 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