LiquiBand Flex

GUDID 05036912000925

ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

Skin-approximation adhesive

• Primary Device ID: 05036912000925
• NIH Device Record Key: 5870abb4-b33d-4b17-b267-5b9c509c4eb1
• Commercial Distribution Discontinuation: 2018-12-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: LiquiBand Flex
• Version Model Number: LBF001
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05036912000529 [Package]; Contains: 05036912000697; Package: Carton [10 Units]; Discontinued: 2018-12-28; Not in Commercial Distribution
GS1	05036912000697 [Primary]
GS1	05036912000925 [Package]; Contains: 05036912000529; Package: Shipper Carton [6 Units]; Discontinued: 2018-12-28; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102076

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: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2018-12-28
• Device Publish Date: 2016-09-06

On-Brand Devices [LiquiBand Flex]

• 05036912000932: LBF006
• 05036912000925: LBF001