Basik

GUDID 00810126505378

BASIK PDO USP 1 1/2 CIRC REV CUTTING NEEDLE 36 MM

3D DENTAL DESIGNS AND DEVELOPMENT, LLC

Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 00810126505378
• NIH Device Record Key: 524f3295-6169-4c69-8277-2d23f4edef39
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Basik
• Version Model Number: BPDO468
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810126505378 [Primary]
GS1	10810126505375 [Package]; Package: Box/12 [12 Units]; In Commercial Distribution

FDA Product Code

• NEW: Suture, Surgical, Absorbable, Polydioxanone

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