NA (UDI RDT2.8L45D)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: RDT2.8L45D) is a medical device manufactured by NEWCLIP TECHNICS. This product is indexed under FDA Product Code / Category Classification HWC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RDT2.8L45D
Product Code / EMDN: HWC
Device Name
Database Sync Date: 2026-08-09 09:00:28

Full Regulatory Attributes

🔒 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 NA?

The registered manufacturer of record for NA is NEWCLIP TECHNICS.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RDT2.8L45D.

What classification code is assigned to this device?

This device is registered under product classification code HWC.

Similar Classification Devices (HWC)

Other Devices by NEWCLIP TECHNICS

Programmatic Export

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

JSON API Endpoint