NuvoMed

GUDID 04719871820322

NuvoMed Wireless Glucose Monitor

BIOTEST MEDICAL CORPORATION

Glucose monitoring system IVD, home-use

• Primary Device ID: 04719871820322
• NIH Device Record Key: e5ae36d6-01b4-4a1b-842c-6f52f9dfb411
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NuvoMed
• Version Model Number: P5228 BGM-6/0352
• Company DUNS: 658447255
• Company Name: BIOTEST MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719871820322 [Primary]

FDA Product Code

• NBW: System, Test, Blood Glucose, Over The Counter

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: 2018-04-09
• Device Publish Date: 2018-03-07

On-Brand Devices [NuvoMed ]

• 04719871820322: NuvoMed Wireless Glucose Monitor
• 04719871820315: NuvoMed Wireless Blood Glucose Monitoring System