FEELject Disposable syringe

GUDID 18809407788660

Feeltech Co.,Ltd.

General-purpose syringe, single-use

• Primary Device ID: 18809407788660
• NIH Device Record Key: d2212fb0-3454-45cb-b2a1-55347e8e971f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FEELject Disposable syringe
• Version Model Number: 1mL/cc x FDN3
• Company DUNS: 688432407
• Company Name: Feeltech Co.,Ltd.
• Device Count: 100
• 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	08809407788663 [Primary]
GS1	08809407789103 [Unit of Use]
GS1	18809407788660 [Package]; Contains: 08809407788663; Package: Cartonbox [3000 Units]; In Commercial Distribution

FDA Product Code

• FMF: Syringe, Piston

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: 2021-07-01
• Device Publish Date: 2021-06-23

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