GUDIDData
eudamed_udi Primary ID: 00840106905997

ME-060-03-74 12" ME w/ Female Luers (UDI 00840106905997)

Manufactured by Perma Pure, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ME-060-03-74 12" ME w/ Female Luers - Primary ID 00840106905997

Device Regulatory Overview

The ME-060-03-74 12" ME w/ Female Luers (Model/Catalog Number: ME-060-03-74) 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-060-03-74
Product Code / EMDN
R9080
Device Name
Nafionβ„’ Tube Dryer, ME Series
Database Sync Date
2026-08-09 17:58:51

Full Regulatory Attributes

πŸ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of ME-060-03-74 12" ME w/ Female Luers?

The registered manufacturer of record for ME-060-03-74 12" ME w/ Female Luers is Perma Pure, LLC.

What is the Primary UDI-DI identifier for ME-060-03-74 12" ME w/ Female Luers?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840106905997.

What classification code is assigned to this device?

This device is registered under product classification code R9080.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint