lansinoh

GUDID 26973493592438

Shenzhen TPH Technology Co., Ltd

Breast pump, electric

• Primary Device ID: 26973493592438
• NIH Device Record Key: 03dfad1d-0706-4011-841b-005873db2c01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: lansinoh
• Version Model Number: P3
• Company DUNS: 403304567
• Company Name: Shenzhen TPH Technology 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	16973493592431 [Primary]
GS1	26973493592438 [Package]; Contains: 16973493592431; Package: [8 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250350

FDA Product Code

• HGX: Pump, Breast, Powered

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: 2026-03-05
• Device Publish Date: 2026-02-25

On-Brand Devices [lansinoh ]

• 16973493593766: S32-D
• 26973493592438: P3