nixit

GUDID 00627987071368

Nixit Limited

Menstrual cup, non-latex, reusable

• Primary Device ID: 00627987071368
• NIH Device Record Key: 7cd830b3-a311-4ef8-a56d-9cb74027e9a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: nixit
• Version Model Number: 00627987071368
• Company DUNS: 204591013
• Company Name: Nixit Limited
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00627987071368 [Primary]

FDA Product Code

• HHE: Cup, Menstrual

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

[00627987071368]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-08
• Device Publish Date: 2019-01-08