CryoRx KRP/MYY-B6-M

GUDID 06973641888488

Pulse Cold Compression Therapy System - Shoulder Cuff

Chengdu Cryo-push Medical Technology Co.,Ltd.

Circulating-fluid localized thermal therapy system pack, reusable

• Primary Device ID: 06973641888488
• NIH Device Record Key: 5114a212-b22d-46d1-8e02-fecae640dd8e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CryoRx
• Version Model Number: D-KRP/MYY-B6-M
• Catalog Number: KRP/MYY-B6-M
• Company DUNS: 543049236
• Company Name: Chengdu Cryo-push Medical 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973641888488 [Primary]

FDA Product Code

• ILO: Pack, Hot Or Cold, Water Circulating

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-11-24
• Device Publish Date: 2025-09-16

On-Brand Devices [CryoRx]

• 06973641888518: Pulse Cold Compression Therapy System - Main Unit
• 06973641888501: Pulse Cold Compression Therapy System - Knee Cuff
• 06973641888495: Pulse Cold Compression Therapy System - Back Cuff
• 06973641888488: Pulse Cold Compression Therapy System - Shoulder Cuff
• 06973641888471: Pulse Cold Compression Therapy System - Ankle Cuff