DEEP OSCILLATION® Personal

GUDID 04099649000010

PHYSIOMED ELEKTROMEDIZIN AG

Hand-held electric massager

• Primary Device ID: 04099649000010
• NIH Device Record Key: e82002c0-35b9-4bd2-a035-7f51d137508a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DEEP OSCILLATION® Personal
• Version Model Number: DOP1.1
• Company DUNS: 316105386
• Company Name: PHYSIOMED ELEKTROMEDIZIN AG
• 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: 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	04099649000010 [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: 2024-01-09
• Device Publish Date: 2024-01-01

Devices Manufactured by PHYSIOMED ELEKTROMEDIZIN AG

• 04099649000010 - DEEP OSCILLATION® Personal: 2024-01-09
• 04099649000010 - DEEP OSCILLATION® Personal: 2024-01-09
• 04099649000041 - DEEP OSCILLATION® Evident: 2024-01-09
• 04099649000058 - HIVAMAT®200 PERSONAL: 2024-01-09
• 04099649000065 - HIVAMAT®200 EVIDENT: 2024-01-09