LIFECHEK

GUDID 06947656110353

Guangzhou Berrcom Medical Device Co., Ltd

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• Primary Device ID: 06947656110353
• NIH Device Record Key: 5a72f452-e73b-4b14-8b20-2f993bbe3735
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIFECHEK
• Version Model Number: JXB-188
• 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	06947656110353 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130231

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

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: 2020-02-19
• Device Publish Date: 2020-02-11

On-Brand Devices [LIFECHEK]

• 06947656110353: JXB-188
• 06947656112708: JXB-188
• 16947656113054: JXB-178