Cascade (UDI 910047)
Manufactured by Musculoskeletal Transplant Foundation, Inc.
Device Regulatory Overview
The Cascade (Model/Catalog Number: 910047) is a medical device manufactured by Musculoskeletal Transplant Foundation, Inc.. This product is indexed under FDA Product Code / Category Classification KSS within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 910047
- Product Code / EMDN
- KSS
- Device Name
- Autologous Platelet System - PRP X 2
- 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 Cascade?
The registered manufacturer of record for Cascade is Musculoskeletal Transplant Foundation, Inc..
What is the Primary UDI-DI identifier for Cascade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 910047.
What classification code is assigned to this device?
This device is registered under product classification code KSS.
Similar Classification Devices (KSS)
Other Devices by Musculoskeletal Transplant Foundation, Inc.
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