VEGA

GUDID 16946159500217

VEGA TECHNOLOGIES INC.

Hot/cold therapy pack, reusable

• Primary Device ID: 16946159500217
• NIH Device Record Key: 468ae3cd-5dfd-4f61-91e5-d4ea3ed7325a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VEGA
• Version Model Number: CM-01
• Company DUNS: 421290561
• Company Name: VEGA TECHNOLOGIES INC.
• 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: true
• Expiration Date: true
• 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	06946159503488 [Primary]
GS1	16946159500217 [Package]; Contains: 06946159503488; Package: [4 Units]; In Commercial Distribution
GS1	26946159500016 [Package]; Package: [8 Units]; In Commercial Distribution

FDA Product Code

• IME: Pack, Hot Or Cold, Reusable

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: 2024-05-21
• Device Publish Date: 2024-05-13

On-Brand Devices [VEGA]

• 06946159501484: CM-01
• 06946159505024: MT-218
• 16946159500217: CM-01