Trubond

GUDID 08903837199003

HEALTHIUM MEDTECH LIMITED

Polyolefin/fluoropolymer suture, monofilament

• Primary Device ID: 08903837199003
• NIH Device Record Key: 5fb1a2d1-80f1-42f9-9cfd-01cfe7407516
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trubond
• Version Model Number: 6D75CX30
• Company DUNS: 916326705
• Company Name: HEALTHIUM MEDTECH 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08903837199003 [Primary]

FDA Product Code

• GAT: Suture, Nonabsorbable, Synthetic, Polyethylene

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: 2024-07-18
• Device Publish Date: 2024-07-10

On-Brand Devices [Trubond]

• 08903837199003: 6D75CX30
• 08903837021427: 6E75CX24
• 08903837298119: ED250209