Basik

GUDID 00817169022985

Basik PGLA USP 4/0 - 3/8 Rev cut 19mm

3D DENTAL DESIGNS AND DEVELOPMENT, LLC

Polyester suture, bioabsorbable, multifilament, non-antimicrobial

• Primary Device ID: 00817169022985
• NIH Device Record Key: a6bf752c-ea1c-4c7b-b0ab-0c173ebab8bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Basik
• Version Model Number: BPGLA397
• Company DUNS: 080194935
• Company Name: 3D DENTAL DESIGNS AND DEVELOPMENT, LLC
• 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	00817169022985 [Primary]
GS1	10817169022982 [Package]; Package: Box/12 [12 Units]; In Commercial Distribution

FDA Product Code

• GAM: Suture, Absorbable, Synthetic, Polyglycolic Acid

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: 2026-03-13
• Device Publish Date: 2026-03-05

On-Brand Devices [Basik]

• 10817169023033: Blue Nylon Monofilament Sutures 3/0 3/8cut 24mm
• 10817169023026: Blue Nylon Monofilament Sutures 2/0 3/8cut 26mm
• 00817169023012: Baskik PGLA USP 0 - 1/2 circle Revcut 36mm
• 00817169022992: Basik PGLA USP 3/0 - 3/8 Rev cut 24mm
• 00817169022985: Basik PGLA USP 4/0 - 3/8 Rev cut 19mm
• 00810126505378: BASIK PDO USP 1 1/2 CIRC REV CUTTING NEEDLE 36 MM