Rejubeau Extra Fine Cannula 27G x 50mm

GUDID 28800145508418

Feeltech Co.,Ltd.

Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 28800145508418
• NIH Device Record Key: f47df943-2f65-4a23-a085-696b5a13fe24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rejubeau Extra Fine Cannula 27G x 50mm
• Version Model Number: FTMN27-50
• Company DUNS: 688432407
• Company Name: Feeltech Co.,Ltd.
• Device Count: 24
• 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	08800145508414 [Unit of Use]
GS1	18800145508411 [Primary]
GS1	28800145508418 [Package]; Contains: 18800145508411; Package: carton box [1200 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172602

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen
• NEW: Suture, Surgical, Absorbable, Polydioxanone

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: 2024-05-17
• Device Publish Date: 2024-05-09

Devices Manufactured by Feeltech Co.,Ltd.

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• 28800145521974 - V-Soft Line ARTE 18Gx100mm FDA: 2026-02-02
• 28800145522056 - V-Soft Line ARTE 19Gx100mm FDA: 2026-02-02
• 28800145522414 - V-Soft Line ARTE3 17Gx70mm FDA: 2026-02-02