eudamed_udi
Primary ID: 00810020360028
Unspecified Brand (UDI 00810020360028)
Manufactured by Perma Pure, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 00810020360028
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: ME-050-03-243) 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-050-03-243
- Product Code / EMDN
- R9080
- Device Name
- Nafion™ Tube Dryer, ME Series
- Database Sync Date
- 2026-08-09 17:17:31
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Perma Pure, LLC.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810020360028.
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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