Nuvaderm

GUDID 00086634900040

CHESSON LABORATORY ASSOCIATES, INC

First aid gauze/bandage

• Primary Device ID: 00086634900040
• NIH Device Record Key: 06e0e296-3a12-4402-8166-e3f62805e8bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nuvaderm
• Version Model Number: Non-Sterile
• Company DUNS: 946203481
• Company Name: CHESSON LABORATORY ASSOCIATES, INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does n
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• 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	00086634900040 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K083913

FDA Product Code

• KMF: Bandage, Liquid

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: 2018-07-30
• Device Publish Date: 2018-06-28

On-Brand Devices [Nuvaderm]

• 00086634900040: Non-Sterile
• 00866349000404: Non-Sterile