Ou Nuo

GUDID 06975683900029

Changzhou Ou Nuo Medical Equipment Co., Ltd.

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• Primary Device ID: 06975683900029
• NIH Device Record Key: 8715d891-022b-4e5e-92af-955eea24d1c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ou Nuo
• Version Model Number: T050RC125N
• Company DUNS: 723688236
• Company Name: Changzhou Ou Nuo Medical Equipment 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	06975683900029 [Primary]

FDA Product Code

• EBH: Material, Impression Tray, Resin

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: 2023-03-03
• Device Publish Date: 2023-02-23

On-Brand Devices [Ou Nuo]

• 06975683900012: T040RC125N
• 06975683900067: T100RC125N
• 06975683900050: T088RC125N
• 06975683900043: T076RC125N
• 06975683900036: T063RC125N
• 06975683900029: T050RC125N