Crutch

GUDID 06972223254727

Foshan Shunkangda Medical Tech Co.,Ltd

Single-base walking stick

• Primary Device ID: 06972223254727
• NIH Device Record Key: 8340eaeb-2625-40dd-839d-df7bd6cba091
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Crutch
• Version Model Number: CA8012LXS
• Company DUNS: 527141834
• Company Name: Foshan Shunkangda Medical Tech 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: 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	06972223254727 [Primary]

FDA Product Code

• IPR: Crutch

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: 2025-07-25
• Device Publish Date: 2025-07-17

On-Brand Devices [Crutch]

• 06972223254697: CA8012LL
• 06972223254734: CA8062L
• 06972223254727: CA8012LXS
• 06972223254710: CA8012LS
• 06972223254703: CA8012LM