STA R Max®

GUDID 03607450590265

DIAGNOSTICA STAGO

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• Primary Device ID: 03607450590265
• NIH Device Record Key: d6ff690a-4515-4d03-93c8-3e084dcccd9f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STA R Max®
• Version Model Number: 59026
• Company DUNS: 262277122
• Company Name: DIAGNOSTICA STAGO
• 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: true
• 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	03607450590265 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082675

FDA Product Code

• JPA: SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES

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: 2022-09-16
• Device Publish Date: 2018-10-30

On-Brand Devices [STA R Max®]

• 03607450590265: 59026
• 03607450590135: 59013