Morpilot

GUDID 06951740501644

Shenzhen Jumper Medical Equipment Co.,Ltd.

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• Primary Device ID: 06951740501644
• NIH Device Record Key: d14ad772-9068-4627-8fa4-810a7e52fb02
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Morpilot
• Version Model Number: JPD-FR401
• Company DUNS: 529217911
• Company Name: Shenzhen Jumper Medical Equipment 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: 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	06951740501644 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131243

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-05-19

Devices Manufactured by Shenzhen Jumper Medical Equipment Co.,Ltd.

• 06951740500654 - H-E-B inControl: 2023-12-14
• 06951740517959 - PUREMED: 2023-12-12
• 06951740520133 - Jumper: 2023-11-28
• 06951740520140 - Jumper: 2023-11-28
• 06951740500647 - Misure: 2023-11-27
• 06951740500593 - JUMPER: 2023-11-13
• 06951740517904 - JUMPER: 2023-11-13
• 06951740500586 - JUMPER: 2023-11-08