Revive RVT30

GUDID EJKP100003960A0

JK-Products GmbH

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• Primary Device ID: EJKP100003960A0
• NIH Device Record Key: 21245c33-bd38-47ea-9240-3e53424d7696
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Revive RVT30
• Version Model Number: JK 98 / BA VBR E
• Company DUNS: 316232073
• Company Name: JK-Products GmbH
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EJKP100003960A0 [Primary]

FDA Product Code

• BXB: Exerciser, Powered

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: 2023-05-08
• Device Publish Date: 2023-04-30

On-Brand Devices [Revive RVT30]

• EJKP100003960A0: JK 98 / BA VBR E
• EJKP100003960B0: JK 98 / RV 30-0 VBR E