Knob

GUDID 16948538362775

Knob

BMC Medical Co., Ltd.

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• Primary Device ID: 16948538362775
• NIH Device Record Key: 9318cc4f-8c25-409f-aa9f-07c274fceb13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Knob
• Version Model Number: NA
• Company DUNS: 526010310
• Company Name: BMC Medical Co., Ltd.
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06948538362778 [Primary]
GS1	16948538362775 [Package]; Contains: 06948538362778; Package: [400 Units]; In Commercial Distribution

FDA Product Code

• BZD: Ventilator, Non-Continuous (Respirator)

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: 2022-11-10
• Device Publish Date: 2022-09-15

On-Brand Devices [Knob]

• 16948538362775: Knob
• 16948538362768: Knob