NL400

GUDID 04560264573260

NAKANISHI INC.

Surgical power tool system control unit, line-powered

• Primary Device ID: 04560264573260
• NIH Device Record Key: 621557d0-34c6-4d00-b22b-8c0b04ed3d53
• Commercial Distribution Discontinuation: 2023-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: NL400
• Version Model Number: TI-MAX NL400 CONTROL BOX
• Company DUNS: 690710546
• Company Name: NAKANISHI INC.
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	04560264573260 [Primary]

FDA Product Code

• EBW: Controller, foot, handpiece and cord

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-09-04
• Device Publish Date: 2020-09-18

On-Brand Devices [NL400]

• 04560224989254: NL400CDB
• 04560224989230: NL400MCB
• 04560224989223: NL400CMC
• 04560264574038: NL400SBSET2BEL
• 04560264573772: NL400S120E
• 04560264573260: TI-MAX NL400 CONTROL BOX
• 04560264572959: NL400CDE
• 04560264572850: NL400
• 04560264572843: NL400CD