NGB-036 Needle-guided Bracket

GUDID 06944904093093

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking holder, reusable Ultrasound imaging system tracking positioner, reusable Ultrasound imaging system tracking positioner, reusable Ultrasound imaging system tracking positioner, reusable Ultrasound imaging system tracking positioner, reusable Ultrasound imaging system tracking positioner, reusable Ultrasound imaging system tracking positioner, reusable

• Primary Device ID: 06944904093093
• NIH Device Record Key: 19aeb6e4-b287-42a5-9548-5c69a09215ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NGB-036 Needle-guided Bracket
• Version Model Number: 120-004741-00
• Company DUNS: 654671304
• Company Name: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	06944904093093 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171233

FDA Product Code

• ITX: Transducer, Ultrasonic, Diagnostic

Sterilization

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

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

[06944904093093]

Hydrogen Peroxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-12-23
• Device Publish Date: 2018-08-03

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