MINIMLL MINI05

GUDID 66941845202852

0.5ML LUER LOCK SYRINGE

AIR-TITE PRODUCTS COMPANY, INC.

Metered-delivery hypodermic syringe

• Primary Device ID: 66941845202852
• NIH Device Record Key: f77d949c-a907-4da0-a6ef-27590326cff6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MINIMLL
• Version Model Number: MINI05
• Catalog Number: MINI05
• Company DUNS: 002385425
• Company Name: AIR-TITE PRODUCTS COMPANY, INC.
• Device Count: 100
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM
• Phone: 7573402501
• Email: ATINFO@AIR-TITE.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	06941845203635 [Unit of Use]
GS1	16941845201843 [Primary]
GS1	66941845202852 [Package]; Contains: 16941845201843; Package: CASE [20 Units]; In Commercial Distribution

FDA Product Code

• FMF: Syringe, Piston

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: 2023-12-07
• Device Publish Date: 2023-11-29

Devices Manufactured by AIR-TITE PRODUCTS COMPANY, INC.

• 20850017403363 - EZ FLO: 2023-12-07 HYPODERMIC NEEDLE 18G X 3/4"
• 66941845202852 - MINIMLL: 2023-12-070.5ML LUER LOCK SYRINGE
• 66941845202852 - MINIMLL: 2023-12-07 0.5ML LUER LOCK SYRINGE
• 20850017403004 - EZ FLO: 2020-04-23 HYPODERMIC NEEDLE 15G X 1-1/2"
• 20850017403011 - EZ FLO: 2020-04-23 HYPODERMIC NEEDLE 16G X 1"
• 20850017403028 - EZ FLO: 2020-04-23 HYPODERMIC NEEDLE 16G X 1-1/2"
• 20850017403035 - EZ FLO: 2020-04-23 HYPODERMIC NEEDLE 17G X 2"
• 20850017403042 - EZ FLO: 2020-04-23 HYPODERMIC NEEDLE 18G X 1"
• 20850017403059 - EZ FLO: 2020-04-23 HYPODERMIC NEEDLE 18G X 1-1/2"