Copper Compression

GUDID 06976093320018

Harvest Spf Textile (Beijing) Co.,Ltd

Hand-held electric massager

• Primary Device ID: 06976093320018
• NIH Device Record Key: a82abbb0-1129-4c21-8879-652604f54bb4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Copper Compression
• Version Model Number: CCVBKE
• Company DUNS: 526874366
• Company Name: Harvest Spf Textile (Beijing) 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06976093320018 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2023-09-19
• Device Publish Date: 2023-09-11

On-Brand Devices [Copper Compression]

• 06976093320001: OS
• 06976093320032: CCCVBG
• 06976093320025: CCVBBW
• 06976093320018: CCVBKE