Neteera 130H US Kit (DRZ)

GUDID 07290117120026

NETEERA TECHNOLOGIES LTD

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• Primary Device ID: 07290117120026
• NIH Device Record Key: ca53efa9-2e80-47f6-838e-463c4b01aed5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neteera 130H US Kit (DRZ)
• Version Model Number: 130-00-102-00
• Company DUNS: 600710452
• Company Name: NETEERA TECHNOLOGIES LTD
• 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: 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	07290117120026 [Primary]

FDA Product Code

• DRZ: Oscillometer

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-24
• Device Publish Date: 2021-11-16