Fine Micro Cannula Fine Micro Cannula 22Gx50mm

GUDID 28809407786458

Feeltech Co.,Ltd.

Hypodermic needle, single-use

• Primary Device ID: 28809407786458
• NIH Device Record Key: cfc42045-3052-46c3-8408-67d840b4a255
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fine Micro Cannula
• Version Model Number: FTMN22-50-21
• Catalog Number: Fine Micro Cannula 22Gx50mm
• 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: 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	08809407786454 [Unit of Use]
GS1	18809407786451 [Primary]
GS1	28809407786458 [Package]; Contains: 18809407786451; Package: [1200 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092831

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-10-23
• Device Publish Date: 2019-09-22

On-Brand Devices [Fine Micro Cannula]

• 28809407786526: FTMN30-25-27
• 28809407786519: FTMN27-50-26
• 28809407786502: FTMN27-40-26
• 28809407786496: FTMN27-25-26
• 28809407786489: FTMN25-50-23
• 28809407786472: FTMN25-40-23
• 28809407786465: FTMN22-70-21
• 28809407786458: FTMN22-50-21