HOMLAND

GUDID 04895262504016

HongKong Pishon Medical Equipment Co., Limited

Handgrip disability-assistive walker, non-powered, non-foldable

• Primary Device ID: 04895262504016
• NIH Device Record Key: f45e057b-835b-48b5-b706-18bb0aba5374
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HOMLAND
• Version Model Number: R2-RD
• Company DUNS: 989225520
• Company Name: HongKong Pishon Medical Equipment Co., Limited
• 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: 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	04895262504016 [Primary]

FDA Product Code

• ITJ: Walker, Mechanical

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: 2026-02-03
• Device Publish Date: 2026-01-26