IMPROSAFE® Blood Collection Set with Pre-Attached Holder 596125302

GUDID 26974481831041

Guangzhou Improve Medical Instruments Co., Ltd.

Blood collection set, invasive

• Primary Device ID: 26974481831041
• NIH Device Record Key: 62a7920d-b3be-4fca-a256-8977915a565b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMPROSAFE® Blood Collection Set with Pre-Attached Holder
• Version Model Number: 25G×3/4”×12”
• Catalog Number: 596125302
• Company DUNS: 554555378
• Company Name: Guangzhou Improve Medical Instruments Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	06974481831047 [Primary]
GS1	26974481831041 [Package]; Contains: 06974481831047; Package: [25 Units]; In Commercial Distribution
GS1	76974481831046 [Package]; Package: 8(25*8) [200 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153388

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

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: 2025-03-24
• Device Publish Date: 2025-03-14

On-Brand Devices [IMPROSAFE® Blood Collection Set with Pre-Attached Holder]

• 16974481831075: 23G x 3/4” x 7”
• 16974481831037: 23G x 3/4” x 12”
• 06974481831023: 21G×3/4”×12”
• 26974481831058: 27G×2/5”×12”
• 26974481831041: 25G×3/4”×12”