INNOSET

GUDID 10857182006019

SAFETY BLOOD COLLECTION SET 23G

INNOVATIVE MEDICAL TECHNOLOGIES, INC

Venous butterfly needle/set

• Primary Device ID: 10857182006019
• NIH Device Record Key: ec7cfd7e-76cf-4c3d-908d-273e7034da17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INNOSET
• Version Model Number: 596123
• Company DUNS: 792740578
• Company Name: INNOVATIVE MEDICAL TECHNOLOGIES, INC
• Device Count: 50
• 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: false
• 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

Device Dimensions

• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857182006012 [Unit of Use]
GS1	10857182006019 [Primary]
GS1	20857182006016 [Package]; Package: CASE [4 Units]; In Commercial Distribution

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-06-06

On-Brand Devices [INNOSET]

• 20857182006023: SAFETY BLOOD COLLECTION SET 25G
• 10857182006019: SAFETY BLOOD COLLECTION SET 23G
• 20857182006009: SAFETY BLOOD COLLECTION SET 21G