DLIR

GUDID 00195278303202

DLIR Application Container for Smart Subscription

GE HEALTHCARE JAPAN CORPORATION

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• Primary Device ID: 00195278303202
• NIH Device Record Key: 7af0fad3-aba9-4274-a0e8-99254037dbb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DLIR
• Version Model Number: 1.1
• Company DUNS: 696021596
• Company Name: GE HEALTHCARE JAPAN 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	00195278303202 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193170

FDA Product Code

• JAK: System, x-ray, tomography, computed

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: 2021-09-02
• Device Publish Date: 2021-08-25

On-Brand Devices [DLIR]

• 00840682146586: 1.0
• 00195278303202: DLIR Application Container for Smart Subscription
• 00195278620453: SWMD DLIR Application for Smart Subscription