SANPU

GUDID 00739810203973

Shenzhen Lingku Ecommerce Co., Ltd.

Intermittent electronic patient thermometer

• Primary Device ID: 00739810203973
• NIH Device Record Key: f7de94cf-89bd-462b-a8d5-bc7cdd1890f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SANPU
• Version Model Number: FDTH-VO-4
• 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: false
• 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	00739810203973 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072641

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: 2017-05-11

On-Brand Devices [SANPU]

• 00667673872824: JPD-FR408
• 00667673872725: FDIR-V5
• 00739810203973: FDTH-VO-4