ULTRAFLO-A 902

GUDID 00857182006296

MALE LUER ACCESS DEVICE

INNOVATIVE MEDICAL TECHNOLOGIES, INC

Blood collection set, noninvasive

• Primary Device ID: 00857182006296
• NIH Device Record Key: ed60f7c9-e5b5-456b-8d5a-d4273ac748d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRAFLO-A
• Version Model Number: 902
• Catalog Number: 902
• Company DUNS: 792740578
• Company Name: INNOVATIVE MEDICAL TECHNOLOGIES, INC
• Device Count: 200
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM
• Phone: 8665201820
• Email: SUPPORT@INNOVATIVEMEDTECH.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857182006296 [Unit of Use]
GS1	20857182006290 [Primary]

FDA Product Code

• KST: System, Blood Collection, Vacuum-Assisted, Manual

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: 2025-02-24
• Device Publish Date: 2025-02-14

Devices Manufactured by INNOVATIVE MEDICAL TECHNOLOGIES, INC

• 00857182006173 - ULTRAFLO-S: 2025-02-24 SAFETY BLOOD COLLECTION SET 23GX3/4X12"
• 00857182006326 - ULTRAFLO-S: 2025-02-24 SAFETY BLOOD COLLECTION SET 21Gx3/4x12"
• 00857182006289 - ULTRAFLO-T: 2025-02-24 FEMALE LUER BLOOD TRANSFER DEVICE
• 00857182006296 - ULTRAFLO-A: 2025-02-24MALE LUER ACCESS DEVICE
• 00857182006296 - ULTRAFLO-A: 2025-02-24 MALE LUER ACCESS DEVICE
• 00857182006333 - ULTRAFLO-S: 2025-02-24 SAFETY BLOOD COLLECTION SET 25GX3/4X12"
• 00857182006197 - ULTRAFLO-V: 2025-02-21 SAFETY BLOOD COLLECTION NEEDLE 21GX1.25"
• 00857182006258 - ULTRAFLO-R: 2025-02-21 PUSH BUTTON SAFETY BLOOD COLLECTION AND INFUSION SET 21GX3/4"X7" W LUER ADAPTER
• 00857182006616 - ULTRAFLO-R: 2025-02-21 PUSH BUTTON SAFETY BLOOD COLLECTION AND INFUSION SET 23GX3/4"X7" W LUER ADAPTER