STERiJECT TM

GUDID 14571225314379

TSK STERiJECT Premium Disposable Hypodermic Needle

TSK LABORATORY, JAPAN

Hypodermic needle, single-use

• Primary Device ID: 14571225314379
• NIH Device Record Key: 4a9f97a2-a3c7-4ceb-90f4-4e0aeae67129
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERiJECT TM
• Version Model Number: PRC-27025ISG
• Company DUNS: 716217877
• Company Name: TSK LABORATORY, JAPAN
• 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: false
• 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: true

Device Dimensions

• Length: 25 Millimeter
• Length: 25 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04571225314372 [Package]; Contains: 04571225314488; Package: Box [40 Units]; In Commercial Distribution
GS1	04571225314488 [Primary]
GS1	14571225314379 [Package]; Contains: 04571225314372; Package: Carton [75 Units]; In Commercial Distribution
GS1	14571225314485 [Package]; Contains: 04571225314488; Package: Carton [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970370

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: 5
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-12-23

On-Brand Devices [STERiJECT TM]

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