NOVA

GUDID 06951740540360

Shenzhen Jumper Medical Equipment Co.,Ltd.

Pulse oximeter

• Primary Device ID: 06951740540360
• NIH Device Record Key: 32e91f32-8503-4f20-8c4d-0d74b75e8214
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NOVA
• Version Model Number: PO-301
• 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	06951740540360 [Primary]

FDA Product Code

• DQA: Oximeter
• OCH: Oximeter, Infrared, Sporting, Aviation

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: 2025-08-15
• Device Publish Date: 2025-08-07

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

• 06951740540360 - NOVA: 2025-08-15
• 06951740540360 - NOVA: 2025-08-15
• 06951740518147 - JUMPER: 2025-05-19
• 06951740520188 - JUMPER: 2025-05-19
• 06951740500562 - JUMPER: 2025-04-10
• 06951740500579 - JUMPER: 2025-04-10
• 06951740517935 - JUMPER: 2025-04-10
• 06951740517942 - JUMPER: 2025-04-10
• 06951740520171 - JUMPER: 2025-02-17