Trulon

GUDID 08903837042842

HEALTHIUM MEDTECH LIMITED

Nylon suture, non-bioabsorbable, monofilament

• Primary Device ID: 08903837042842
• NIH Device Record Key: 2773d455-7d27-4bf1-af7d-bfcd2b0278aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trulon
• Version Model Number: 3F75AX60
• 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	08903837042842 [Primary]

FDA Product Code

• GAR: Suture, Nonabsorbable, Synthetic, Polyamide

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: 2025-02-24
• Device Publish Date: 2025-02-16

On-Brand Devices [Trulon]

• 08903837039644: 5G45CX19
• 08903837212412: 15I45CX13
• 08903837044563: 3I45CX11
• 08903837278883: 3E75AX60
• 08903837042842: 3F75AX60