Medela

GUDID 00020451905389

Melody InBra Resupply Kit

Guangdong Youmeng Electrical Technology Co., Ltd.

Breast pump, electric

• Primary Device ID: 00020451905389
• NIH Device Record Key: 7c9d62d6-9c1a-4f85-be8a-073962e771f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medela
• Version Model Number: Melody InBra Resupply Kit
• Company DUNS: 714437286
• Company Name: Guangdong Youmeng Electrical Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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	00020451905389 [Primary]

FDA Product Code

• OHH: Breast Pump Kit

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: 2026-03-30
• Device Publish Date: 2026-03-20

On-Brand Devices [Medela]

• 86978342980086: Wearable electric breast pump
• 00020451905389: Melody InBra Resupply Kit