AGUPUNT IPEN

GUDID 18437016482329

Physiotherapy needles

AGU PUNT SL

Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle Dry-needling needle

• Primary Device ID: 18437016482329
• NIH Device Record Key: 7ae046bc-bd4d-479f-b82c-1950b1ab54bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AGUPUNT IPEN
• Version Model Number: A1008AE
• Company DUNS: 476185710
• Company Name: AGU PUNT SL
• Device Count: 200
• 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	08437016482322 [Primary]
GS1	18437016482329 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K003748

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: 2022-05-05
• Device Publish Date: 2022-04-27

On-Brand Devices [AGUPUNT IPEN]

• 18437016482336: Physiotherapy needles
• 18437016482329: Physiotherapy needles
• 18437016482312: Physiotherapy needles
• 18437016482305: Physiotherapy needles
• 18437016482299: Physiotherapy needles
• 18437016482282: Physiotherapy needles