Nakanishi

GUDID B504OMPDS2NL300

Provision

Orthopaedic bur, single-use

• Primary Device ID: B504OMPDS2NL300
• NIH Device Record Key: bef4a634-39a6-4d00-a3a2-6eab38d226e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nakanishi
• Version Model Number: PDS-2NL-30
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504OMPDS2NL300 [Primary]

FDA Product Code

• GFF: Bur, Surgical, General & Plastic Surgery

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: 2026-02-17
• Device Publish Date: 2026-02-09

On-Brand Devices [Nakanishi]

• B504OMPDS2NM300: PDS-2NM-30
• B504OMPDS2DM300: PDS-2DM-30
• B504OMPDSCRAM0: PDS-CRA-M
• B504OMPDS2TD150: PDS-2TD-15
• B504OMPDS2CM500: PDS-2CM-50
• B504OMPDS1D330350: PDS-1D330-35
• B504OMPDS1CD330350: PDS-1CD330-35
• B504OMPDS2NL300: PDS-2NL-30