eudamed_udi
Primary ID: 00840106905614
ME-070-03-49 Arete Custom ME-070-21FFL (UDI 00840106905614)
Manufactured by Perma Pure, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ME-070-03-49 Arete Custom ME-070-21FFL - Primary ID 00840106905614
Device Regulatory Overview
The ME-070-03-49 Arete Custom ME-070-21FFL (Model/Catalog Number: ME-070-03-49) 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-070-03-49
- Product Code / EMDN
- R9080
- Device Name
- Nafion™ Tube Dryer, ME Series
- Database Sync Date
- 2026-08-09 17:14:09
Full Regulatory Attributes
🔒 Token Gated
{
"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-070-03-49 Arete Custom ME-070-21FFL?
The registered manufacturer of record for ME-070-03-49 Arete Custom ME-070-21FFL is Perma Pure, LLC.
What is the Primary UDI-DI identifier for ME-070-03-49 Arete Custom ME-070-21FFL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840106905614.
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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