AccuMax

GUDID 08714729784647

Single-Use Holmium Laser Fiber

BOSTON SCIENTIFIC CORPORATION

General/multiple surgical laser system beam guide, single-use

• Primary Device ID: 08714729784647
• NIH Device Record Key: 46f4e6bb-84b8-41fc-8a58-c41c70be36d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AccuMax
• Version Model Number: M0068404030
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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: false
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729784609 [Primary]
GS1	08714729784647 [Package]; Contains: 08714729784609; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• GEX: Powered laser surgical instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2021-04-07
• Device Publish Date: 2016-09-24

On-Brand Devices [AccuMax]

• 08714729784654: Single-Use Holmium Laser Fiber
• 08714729784647: Single-Use Holmium Laser Fiber
• 08714729784630: Single-Use Holmium Laser Fiber
• 08714729784623: Single-Use Holmium Laser Fiber