PLUG T1

GUDID 18032919891058

Plug T1 7 cm is a macroporous round preshaped flat plug, indicated for the treatment of inguinal hernia defect with open technique

HERNIAMESH SRL

Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

• Primary Device ID: 18032919891058
• NIH Device Record Key: 3a6b9baf-93a9-43e6-9b2a-fe2357eff508
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PLUG T1
• Version Model Number: PT1/7
• Company DUNS: 459310140
• Company Name: HERNIAMESH SRL
• Device Count: 5
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	18032919891058 [Unit of Use]
GS1	58032919891056 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K973955

FDA Product Code

• FTL: Mesh, Surgical, Polymeric

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-08-18
• Device Publish Date: 2023-07-13

On-Brand Devices [PLUG T1]

• 18032919891058: Plug T1 7 cm is a macroporous round preshaped flat plug, indicated for the treatment of inguinal
• 18032919891041: Plug T1 5 cm is a macroporous round preshaped flat plug, indicated for the treatment of inguinal