IDryNeedle 0.30x30

GUDID 28800145508364

Feeltech Co.,Ltd.

Acupuncture needle, single-use

• Primary Device ID: 28800145508364
• NIH Device Record Key: 7d1d83d2-fbdc-43c0-8f0d-824cfdb5f880
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IDryNeedle 0.30x30
• Version Model Number: DNC150 0.30x30
• Company DUNS: 688432407
• Company Name: Feeltech Co.,Ltd.
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: true
• 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	08800145508360 [Unit of Use]
GS1	18800145508367 [Primary]
GS1	28800145508364 [Package]; Contains: 18800145508367; Package: outbox [1000 Units]; In Commercial Distribution
GS1	38800145508361 [Package]; Package: carton box [20000 Units]; In Commercial Distribution

FDA Product Code

• MQX: Needle, Acupuncture, Single Use

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

On-Brand Devices [IDryNeedle 0.30x30]

• 28809407787035: DN150 0.30x30
• 28800145508364: DNC150 0.30x30