PREVE

GUDID 06947656112531

Guangzhou Berrcom Medical Device Co., Ltd

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• Primary Device ID: 06947656112531
• NIH Device Record Key: 7862e5b5-e412-4dad-b9ed-8f7eb8d09c11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PREVE
• Version Model Number: JXB-313
• 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	06947656112531 [Primary]
GS1	36947656112532 [Package]; Package: cartoon [80 Units]; In Commercial Distribution

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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-12-09
• Device Publish Date: 2019-06-04

On-Brand Devices [PREVE]

• 06947656112258: JXB-182
• 06947656111558: JXB-182
• 06947656112531: JXB-313