gudid
Primary ID: PD9700R
Pulsaderm (UDI PD9700R)
Manufactured by PULSADERM LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pulsaderm - Primary ID PD9700R
Device Regulatory Overview
The Pulsaderm (Model/Catalog Number: PD9700R) is a medical device manufactured by PULSADERM LLC. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PD9700R
- Product Code / EMDN
- OLP
- Device Name
- Blue LED Light for the treatment of acne
- Database Sync Date
- 2026-08-09 09:49:20
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Pulsaderm?
The registered manufacturer of record for Pulsaderm is PULSADERM LLC.
What is the Primary UDI-DI identifier for Pulsaderm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PD9700R.
What classification code is assigned to this device?
This device is registered under product classification code OLP.
Similar Classification Devices (OLP)
Other Devices by PULSADERM LLC
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