Rotoflex Blue files S cross section (UDI 21mm pack of six)
Manufactured by PREVEST DENPRO LIMITED
Device Regulatory Overview
The Rotoflex Blue files S cross section (Model/Catalog Number: 21mm pack of six) is a medical device manufactured by PREVEST DENPRO LIMITED. This product is indexed under FDA Product Code / Category Classification EKS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21mm pack of six
- Product Code / EMDN
- EKS
- Device Name
- Database Sync Date
- 2026-08-09 09:01:11
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 Rotoflex Blue files S cross section?
The registered manufacturer of record for Rotoflex Blue files S cross section is PREVEST DENPRO LIMITED.
What is the Primary UDI-DI identifier for Rotoflex Blue files S cross section?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21mm pack of six.
What classification code is assigned to this device?
This device is registered under product classification code EKS.
Similar Classification Devices (EKS)
Other Devices by PREVEST DENPRO LIMITED
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