LPOW

GUDID 00739810204253

Shenzhen Lingku Ecommerce Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 00739810204253
• NIH Device Record Key: 4fb952f8-8f19-4624-b8d8-9cbdff359acb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LPOW
• Version Model Number: JPD-500G
• Company DUNS: 544434375
• Company Name: Shenzhen Lingku Ecommerce 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: false
• 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	00739810204253 [Primary]

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-09-14
• Device Publish Date: 2018-08-14

On-Brand Devices [LPOW]

• 00667673872916: JPD-FR401
• 00739810210599: PG-800B
• 00739810204253: JPD-500G
• 00738629168534: BT-A13