None

GUDID 06971919469032

Ningbo Albert Novosino Co.,Ltd.

Vaginal douche, reusable

• Primary Device ID: 06971919469032
• NIH Device Record Key: 0b965e34-6aba-400d-84f9-1f5a3603e68b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: None
• Version Model Number: 1.0
• Company DUNS: 543014978
• Company Name: Ningbo Albert Novosino 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971919469032 [Primary]

FDA Product Code

• HED: Douche Apparatus, Vaginal, Therapeutic

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: 2022-11-28
• Device Publish Date: 2022-11-18

On-Brand Devices [None]

• 06971919469063: 1.0
• 06971919469056: 1.0
• 06971919469049: 1.0
• 06971919469032: 1.0
• 06971919460817: ED816
• 06971919466949: ER813B