ASTEC IVF 4Well Dish

GUDID 24580647510068

ASTEC CO.,LTD.

Assisted reproduction procedure dish

• Primary Device ID: 24580647510068
• NIH Device Record Key: 08feac88-e70a-4020-baec-79eabd73ed32
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASTEC IVF 4Well Dish
• Version Model Number: AID-4WH
• Company DUNS: 694169152
• Company Name: ASTEC CO.,LTD.
• Device Count: 4
• 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	04580647510064 [Unit of Use]
GS1	14580647510061 [Primary]
GS1	24580647510068 [Package]; Contains: 14580647510061; Package: [30 Units]; In Commercial Distribution

FDA Product Code

• PUD: Labware, Assisted Reproduction, Exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-09
• Device Publish Date: 2024-08-01

On-Brand Devices [ASTEC IVF 4Well Dish]

• 24580647510068: AID-4WH
• 24580647510051: AID-4W