V-Soft Line BARB BLUNT CANNULA L 21Gx90mm FDA

GUDID 28800145521172

Feeltech Co.,Ltd.

Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 28800145521172
• NIH Device Record Key: b27e8b90-d02f-4c04-8f1a-bc00f3e3283a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V-Soft Line BARB BLUNT CANNULA L 21Gx90mm FDA
• Version Model Number: L-FTN2192G
• Company DUNS: 688432407
• Company Name: Feeltech Co.,Ltd.
• Device Count: 5
• 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	08800145521178 [Unit of Use]
GS1	18800145521175 [Primary]
GS1	28800145521172 [Package]; Contains: 18800145521175; Package: INBOX [10 Units]; In Commercial Distribution
GS1	38800145521179 [Package]; Package: CARTONBOX [300 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250107

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: 2026-03-27
• Device Publish Date: 2026-03-19

On-Brand Devices [V-Soft Line BARB BLUNT CANNULA L 21Gx90mm FDA]

• 28800145521530: L4-FTN2192G
• 28800145521172: L-FTN2192G