everActive (UDI 05902020523161)
Manufactured by Baltrade spółka z ograniczoną odpowiedzialnością
Device Regulatory Overview
The everActive (Model/Catalog Number: PR48/13) is a medical device manufactured by Baltrade spółka z ograniczoną odpowiedzialnością. This product is indexed under FDA Product Code / Category Classification Y214580 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PR48/13
- Product Code / EMDN
- Y214580
- Device Name
- everActive Ultrasonic
- Database Sync Date
- 2026-08-09 16:29:09
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 everActive?
The registered manufacturer of record for everActive is Baltrade spółka z ograniczoną odpowiedzialnością.
What is the Primary UDI-DI identifier for everActive?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902020523161.
What classification code is assigned to this device?
This device is registered under product classification code Y214580.
Similar Classification Devices (Y214580)
Other Devices by Baltrade spółka z ograniczoną odpowiedzialnością
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