GUDID 08057509880031

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

INGE SPA

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