Hosmed

GUDID 06942820462184

Pulse Oximeter

Beijing Choice Electronic Technology Co., Ltd.

Pulse oximeter

• Primary Device ID: 06942820462184
• NIH Device Record Key: 35dd83da-086b-45de-9577-6cb0984ad04f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hosmed
• Version Model Number: MD300M
• Company DUNS: 526882823
• Company Name: Beijing Choice Electronic Technology 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942820462184 [Primary]

FDA Product Code

• DQA: Oximeter

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: 2022-07-25
• Device Publish Date: 2022-07-15

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