APS Dry Needling Neeedles

GUDID 08437016482025

AGU PUNT SL

Dry-needling needle

• Primary Device ID: 08437016482025
• NIH Device Record Key: 0a0996a5-9aff-4187-9a50-084ef95b569f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: APS Dry Needling Neeedles
• Version Model Number: A1010P
• Company DUNS: 476185710
• Company Name: AGU PUNT SL
• Device Count: 100
• 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	08437016482025 [Primary]
GS1	18437016482022 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-05-02
• Device Publish Date: 2016-09-29

On-Brand Devices [APS Dry Needling Neeedles]

• 08437016482995: Physiotherapy needles
• 08437016482841: A1048P
• 08437016482544: A1010P-T
• 08437016482193: A1047P-T
• 08437016482186: A1042C-T
• 08437016482162: A1042PS
• 08437016482155: A1038PS
• 08437016482148: A1037PS
• 08437016482131: A1045P
• 08437016482124: A1044P
• 08437016482117: A1043P
• 08437016482100: A1042P
• 08437016482094: A1042CP
• 08437016482087: A1042BP
• 08437016482070: A1041P
• 08437016482063: A1040P
• 08437016482056: A1038P
• 08437016482049: A1037P
• 08437016482032: A1037BP
• 08437016482025: A1010P
• 08437016482018: A1047P