Rejubeau Extra Fine Cannula 23G x 50mm

GUDID 28800145508456

Feeltech Co.,Ltd.

Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 28800145508456
• NIH Device Record Key: d45e1905-5edb-46e3-bd6d-47419d565138
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rejubeau Extra Fine Cannula 23G x 50mm
• Version Model Number: FTMN23G50
• 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	08800145508452 [Unit of Use]
GS1	18800145508459 [Primary]
GS1	28800145508456 [Package]; Contains: 18800145508459; Package: carton box [1200 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172602

FDA Product Code

• 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.

• 28800145508340 - IDryNeedle 0.25x30: 2024-05-17
• 28800145508357 - IDryNeedle 0.25x40: 2024-05-17
• 28800145508364 - IDryNeedle 0.30x30: 2024-05-17
• 28800145508371 - IDryNeedle 0.30x40: 2024-05-17
• 28800145508388 - Rejubeau Extra Fine Cannula 30G x 25mm: 2024-05-17
• 28800145508395 - Rejubeau Extra Fine Cannula 27G x 25mm: 2024-05-17
• 28800145508401 - Rejubeau Extra Fine Cannula 27G x 40mm: 2024-05-17
• 28800145508418 - Rejubeau Extra Fine Cannula 27G x 50mm: 2024-05-17