ME-050-03-275 Custom 050 MGC Diagnostic ME Dryer (UDI 00840106905270)
Manufactured by Perma Pure, LLC
Device Regulatory Overview
The ME-050-03-275 Custom 050 MGC Diagnostic ME Dryer (Model/Catalog Number: ME-050-03-275) is a medical device manufactured by Perma Pure, LLC. This product is indexed under FDA Product Code / Category Classification R9080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ME-050-03-275
- Product Code / EMDN
- R9080
- Device Name
- Nafion™ Tube Dryer, ME Series
- Database Sync Date
- 2026-08-09 16:45:40
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 ME-050-03-275 Custom 050 MGC Diagnostic ME Dryer?
The registered manufacturer of record for ME-050-03-275 Custom 050 MGC Diagnostic ME Dryer is Perma Pure, LLC.
What is the Primary UDI-DI identifier for ME-050-03-275 Custom 050 MGC Diagnostic ME Dryer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840106905270.
What classification code is assigned to this device?
This device is registered under product classification code R9080.
Similar Classification Devices (R9080)
Other Devices by Perma Pure, LLC
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