REA SOUL MAT (UDI 05903699336298)
Manufactured by 313 Spółka z ograniczoną odpowiedzialnością
Device Regulatory Overview
The REA SOUL MAT (Model/Catalog Number: 70) is a medical device manufactured by 313 Spółka z ograniczoną odpowiedzialnością. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 70
- Product Code / EMDN
- Z12069099
- Device Name
- REA SOUL MAT
- Database Sync Date
- 2026-08-09 16:30:10
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 REA SOUL MAT?
The registered manufacturer of record for REA SOUL MAT is 313 Spółka z ograniczoną odpowiedzialnością.
What is the Primary UDI-DI identifier for REA SOUL MAT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903699336298.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by 313 Spółka z ograniczoną odpowiedzialnością
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