FANRY

GUDID 00739810204246

Shenzhen Lingku Ecommerce Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 00739810204246
• NIH Device Record Key: 276cd2df-39de-4065-afb6-672f8cb6ff00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FANRY
• Version Model Number: JPD-500E
• 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	00739810204246 [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: 2018-09-07
• Device Publish Date: 2018-08-07

On-Brand Devices [FANRY]

• 00667673872855: JPD-FR408
• 00739810210971: PG-800B5-1
• 00739810204246: JPD-500E
• 00739810204185: PG-800B27