e-light I-US (UDI 230020148)
Manufactured by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA
Device Regulatory Overview
The e-light I-US (Model/Catalog Number: 230020148) is a medical device manufactured by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA. This product is indexed under FDA Product Code / Category Classification ILY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 230020148
- Product Code / EMDN
- ILY
- Device Name
- Laser system for therapy
- Database Sync Date
- 2026-08-09 09:07:18
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 e-light I-US?
The registered manufacturer of record for e-light I-US is DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA.
What is the Primary UDI-DI identifier for e-light I-US?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 230020148.
What classification code is assigned to this device?
This device is registered under product classification code ILY.
Similar Classification Devices (ILY)
Other Devices by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA
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