GUDID 08057509880031

Kit including 21 cannulas for administering semi-solid preparation into the vagina

INGE SPA

Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable Vaginal applicator, reusable

• Primary Device ID: 08057509880031
• NIH Device Record Key: d91db36b-98b6-425a-9123-4a064100aeaa
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: CO7026
• Company DUNS: 338946150
• Company Name: INGE SPA
• Device Count: 21
• 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: false
• 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	08057509880024 [Unit of Use]
GS1	08057509880031 [Primary]

FDA Product Code

• HGD: Applicator, Vaginal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-08-25
• Device Publish Date: 2022-07-17

Devices Manufactured by INGE SPA

• 08057509880031 - NA: 2022-08-25Kit including 21 cannulas for administering semi-solid preparation into the vagina
• 08057509880031 - NA: 2022-08-25 Kit including 21 cannulas for administering semi-solid preparation into the vagina
• 08057509880024 - NA: 2022-07-25 Cannulas for administering semi-solid preparation into the vagina