gudid Primary ID: RP-U-C12R3

REDPINE (UDI RP-U-C12R3)

Manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The REDPINE (Model/Catalog Number: RP-U-C12R3) is a medical device manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FGB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RP-U-C12R3
Product Code / EMDN: FGB
Device Name
Database Sync Date: 2026-08-09 09:06:41

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 REDPINE?

The registered manufacturer of record for REDPINE is Guangzhou Red Pine Medical Instrument Co., Ltd..

What is the Primary UDI-DI identifier for REDPINE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RP-U-C12R3.

What classification code is assigned to this device?

This device is registered under product classification code FGB.

Similar Classification Devices (FGB)

Other Devices by Guangzhou Red Pine Medical Instrument Co., Ltd.

Programmatic Export

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

JSON API Endpoint