Bahama Hook 0600-1012-000

GUDID 10817984011161

Bahama Hook Metal

MECTRA LABS, INC.

Scalpel, single-use Scalpel, single-use

• Primary Device ID: 10817984011161
• NIH Device Record Key: 6a5f8448-de97-4207-8980-e0a7f77576de
• Commercial Distribution Discontinuation: 2020-01-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Bahama Hook
• Version Model Number: 0600-1012-000
• Catalog Number: 0600-1012-000
• Company DUNS: 606939072
• Company Name: MECTRA LABS, INC.
• Device Count: 1
• DM Exempt: false
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)323-3968
• Email: mectrasales@mectralabs.com
• Phone: +1(800)323-3968
• Email: mectrasales@mectralabs.com

Operating and Storage Conditions

• Handling Environment Temperature: Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
• Handling Environment Temperature: Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817984011164 [Primary]
GS1	10817984011161 [Package]; Contains: 00817984011164; Package: Inner pack [10 Units]; Discontinued: 2020-01-10; Not in Commercial Distribution

FDA Product Code

• LXH: ORTHOPEDIC MANUAL 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: 3
• Public Version Date: 2020-02-06
• Device Publish Date: 2019-01-29

On-Brand Devices [Bahama Hook]

• 10817984011161: Bahama Hook Metal
• 10817984010966: Bahama Hook