LiquiBand XL

GUDID 05036912001397

ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

Wound closure set, topical

• Primary Device ID: 05036912001397
• NIH Device Record Key: 80fde2c9-45c2-48df-9b16-4e8633dd4ff5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiquiBand XL
• Version Model Number: 72014027
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05036912001380 [Primary]
GS1	05036912001397 [Package]; Contains: 05036912001380; Package: Carton [2 Units]; In Commercial Distribution
GS1	05036912001403 [Package]; Package: Shipper Carton [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211878

FDA Product Code

• OMD: Cutaneous Tissue Adhesive With Mesh

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: 2022-06-08
• Device Publish Date: 2022-05-31

On-Brand Devices [LiquiBand XL]

• 05036912001489: 72014046
• 05036912001397: 72014027
• 05036912001243: 72014019
• 05036912001663: 72014046A