AMPMED

GUDID 06947656112142

Guangzhou Berrcom Medical Device Co., Ltd

Intermittent electronic patient thermometer

• Primary Device ID: 06947656112142
• NIH Device Record Key: 3d4c8f20-680e-4759-b331-fc489ca1323a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AMPMED
• Version Model Number: AMP1703
• Company DUNS: 529391821
• Company Name: Guangzhou Berrcom Medical Device 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06947656112142 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163603

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

Sterilization

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

[06947656112142]

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[06947656112142]

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[06947656112142]

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[06947656112142]

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[06947656112142]

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Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-03-11
• Device Publish Date: 2017-12-11

On-Brand Devices [AMPMED]

• 06947656112159: AMP1702
• 06947656112142: AMP1703
• 06947656112135: AMP1703
• 06947656112111: AMP1701
• 06947656111961: AMP1702
• 06947656111954: AMP1701