IMPROVACUTER® Multi Sample Needle 592121250

GUDID 16974481839712

Guangzhou Improve Medical Instruments Co., Ltd.

Blood collection tube holder/needle

• Primary Device ID: 16974481839712
• NIH Device Record Key: b34e72be-ec7b-4fa7-9bb7-4799d499fda1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMPROVACUTER® Multi Sample Needle
• Version Model Number: 21G×1”
• Catalog Number: 592121250
• 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	06974481839715 [Primary]
GS1	16974481839712 [Package]; Contains: 06974481839715; Package: [100 Units]; In Commercial Distribution
GS1	46974481839713 [Package]; Package: 40(100*40) [4000 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 [IMPROVACUTER® Multi Sample Needle]

• 46933395621234: 22G × 1 1/2″
• 46933395621227: 22G × 1″
• 46933395621210: 21G × 1 1/2″
• 46933395621203: 21G × 1″
• 16974481839743: 22G×1 1/2”
• 16974481839736: 22G×1”
• 16974481839729: 21G×1 1/2”
• 16974481839712: 21G×1”