pluse oximeter

GUDID 06951740500265

Shenzhen Jumper Medical Equipment Co.,Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06951740500265
• NIH Device Record Key: 3bee9e6a-aecf-4b97-bbe3-9a84425f26f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: pluse oximeter
• Version Model Number: JPD-500C
• 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	06951740500197 [Primary]
GS1	06951740500265 [Package]; Contains: 06951740500197; Package: [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140582

FDA Product Code

• DQA: Oximeter

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: 2016-09-24

On-Brand Devices [pluse oximeter]

• 06951740540018: pluse oximeter（white）
• 06951740538374: pluse oximeter（white）
• 06951740538367: pluse oximeter（black）
• 06951740500227: JPD-500F
• 06951740500210: JPD-500E
• 06951740500203: JPD-500D
• 06951740500265: JPD-500C
• 06951740500258: JPD-500B
• 06951740500241: JPD-500A
• 06951740540070: SPA30
• 06951740540063: SPA20
• 06951740540056: SPA11
• 06951740540049: SPA10