Homedics

GUDID 06938395500253

Homedics pulse oximeter

Shenzhen Hexin ZONDAN Medical Equipment Co., Ltd

Pulse oximeter

• Primary Device ID: 06938395500253
• NIH Device Record Key: 608d0eb7-b307-4f62-a761-857803fe0f1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Homedics
• Version Model Number: PX-200L
• Company DUNS: 527098717
• Company Name: Shenzhen Hexin ZONDAN Medical Equipment 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06938395500253 [Primary]

FDA Product Code

• PGJ: Oximeter, Wellness

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: 2026-03-23
• Device Publish Date: 2026-03-13