Stradis Healthcare

GUDID M7526821926

General Surgical Kit

STRADIS MEDICAL, LLC

General surgical procedure kit, medicated

• Primary Device ID: M7526821926
• NIH Device Record Key: 5a37aa40-53ca-43a9-a802-bfff56bd9464
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stradis Healthcare
• Version Model Number: 682-1926
• Company DUNS: 174262477
• Company Name: STRADIS MEDICAL, 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: 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

Customer Support Contacts

• Phone: 770-962-2425
• Email: sales@stradishealthcare.com
• Phone: 770-962-2425
• Email: sales@stradishealthcare.com
• Phone: 770-962-2425
• Email: sales@stradishealthcare.com
• Phone: 770-962-2425
• Email: sales@stradishealthcare.com
• Phone: 770-962-2425
• Email: sales@stradishealthcare.com
• Phone: 770-962-2425
• Email: sales@stradishealthcare.com
• Phone: 770-962-2425
• Email: sales@stradishealthcare.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M7526821926 [Primary]

FDA Product Code

• LRO: General Surgery Tray

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: 2019-10-08
• Device Publish Date: 2019-09-30

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