Miracu FC BI 23Gx60mm

GUDID 38809407786745

Feeltech Co.,Ltd.

Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 38809407786745
• NIH Device Record Key: 9247d345-8b59-487f-b6e5-3961b71542fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Miracu FC BI 23Gx60mm
• Version Model Number: F-FTN2363G
• Company DUNS: 688432407
• Company Name: Feeltech Co.,Ltd.
• Device Count: 10
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809407786744 [Unit of Use]
GS1	18809407786741 [Primary]
GS1	28809407786748 [Package]; Contains: 18809407786741; Package: INBOX [10 Units]; In Commercial Distribution
GS1	38809407786745 [Package]; Contains: 28809407786748; Package: CARTON BOX [300 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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-02-05
• Device Publish Date: 2019-12-24

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