Therapy US (FDA) (UDI 980030035)
Manufactured by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA
Device Regulatory Overview
The Therapy US (FDA) (Model/Catalog Number: 980030035) is a medical device manufactured by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA. This product is indexed under FDA Product Code / Category Classification NHN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 980030035
- Product Code / EMDN
- NHN
- 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 Therapy US (FDA)?
The registered manufacturer of record for Therapy US (FDA) is DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA.
What is the Primary UDI-DI identifier for Therapy US (FDA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 980030035.
What classification code is assigned to this device?
This device is registered under product classification code NHN.
Similar Classification Devices (NHN)
Other Devices by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA
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