Dp4

GUDID 08720261027067

Microneedling Device

Equipmed USA B.V.

Cosmetic micro-needling electronic handpiece, professional

• Primary Device ID: 08720261027067
• NIH Device Record Key: af059cfb-a3c9-4f8e-ac6c-98e4f2266b58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dp4
• Version Model Number: DP4-PEN-AX-1
• Company DUNS: 493118351
• Company Name: Equipmed USA B.V.
• Device Count: 1
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	08720261027067 [Primary]

FDA Product Code

• QAI: Powered microneedle device

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-01
• Device Publish Date: 2023-04-21

On-Brand Devices [Dp4]

• 08720261025810: Device Sleeve - Box of 33
• 08720261027067: Microneedling Device
• 08720261022529: Cartridges - Box of 33