STRADIS HEALTHCARE

GUDID M752683126

GENERAL SURGICAL KIT

STRADIS MEDICAL, LLC

General/plastic surgical procedure kit, non-medicated, single-use

• Primary Device ID: M752683126
• NIH Device Record Key: 3fa04951-c40d-4b3b-9ba1-958269142ae6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STRADIS HEALTHCARE
• Version Model Number: 683-126
• 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	M752683126 [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: 2019-11-08
• Device Publish Date: 2019-10-31

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