Nevadent

GUDID 16974637100017

Inwood Electronic Co., Ltd

Oral lavage system

• Primary Device ID: 16974637100017
• NIH Device Record Key: 0a4c633b-1e76-4601-b41c-b7a6079c64ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nevadent
• Version Model Number: NMD 3.7 C8
• Company DUNS: 421175946
• Company Name: Inwood Electronic Co., Ltd
• 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: true
• Serial Number: false
• 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	16974637100017 [Primary]

FDA Product Code

• KAR: Irrigator, Sinus

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: 2023-04-10
• Device Publish Date: 2023-03-31