Sertilac

GUDID 03661522000984

PETERS SURGICAL

Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable Surgical support tape, non-bioabsorbable

• Primary Device ID: 03661522000984
• NIH Device Record Key: 4de2a67e-d27f-4295-ac04-93a4af25118c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sertilac
• Version Model Number: 32300M20
• Company DUNS: 265741780
• Company Name: PETERS SURGICAL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	03661522000984 [Primary]

FDA Product Code

• GAE: Snare, Surgical

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: 2023-06-19
• Device Publish Date: 2023-06-09

Devices Manufactured by PETERS SURGICAL

• 03661522100882 - Applier, hemostatic clip: 2024-01-10
• 03661522100899 - Applier, hemostatic clip: 2024-01-10
• 03661522100905 - Applier, hemostatic clip: 2024-01-10
• 03661522100929 - Applier, hemostatic clip: 2024-01-10
• 03661522100936 - Applier, hemostatic clip: 2024-01-10
• 03661522100912 - Applier, hemostatic clip: 2024-01-05
• 03661522000984 - Sertilac: 2023-06-19
• 03661522000984 - Sertilac: 2023-06-19
• 03661522039540 - Applier, hemostatic clip: 2023-06-16