IDryNeedle 0.25x30

GUDID 28809407787011

Feeltech Co.,Ltd.

Acupuncture needle, single-use

• Primary Device ID: 28809407787011
• NIH Device Record Key: 7190119b-0530-45d9-ac39-73cfb210ea80
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IDryNeedle 0.25x30
• Version Model Number: DN150 0.25x30
• 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: 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	08809407787017 [Unit of Use]
GS1	18809407787014 [Primary]
GS1	28809407787011 [Package]; Contains: 18809407787014; Package: Carton box [20000 Units]; In Commercial Distribution
GS1	38809407787018 [Package]; Package: CARTONBOX [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: 2020-01-23
• Device Publish Date: 2020-01-15

On-Brand Devices [IDryNeedle 0.25x30]

• 28809407787011: DN150 0.25x30
• 28800145508340: DNC150 0.25x30