GUDIDData
eudamed_udi Primary ID: ++G231DE10151033

COMPOSITE PLUGGER INSTRUMENT (UDI ++G231DE10151033)

Manufactured by RAJ IMPEX

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COMPOSITE PLUGGER INSTRUMENT - Primary ID ++G231DE10151033

Device Regulatory Overview

The COMPOSITE PLUGGER INSTRUMENT (Model/Catalog Number: DE-1015-1033) is a medical device manufactured by RAJ IMPEX. This product is indexed under FDA Product Code / Category Classification L159099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DE-1015-1033
Product Code / EMDN
L159099
Device Name
COMPOSITE PLUGGER INSTRUMENT
Database Sync Date
2026-08-09 16:51:36

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 COMPOSITE PLUGGER INSTRUMENT?

The registered manufacturer of record for COMPOSITE PLUGGER INSTRUMENT is RAJ IMPEX.

What is the Primary UDI-DI identifier for COMPOSITE PLUGGER INSTRUMENT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ++G231DE10151033.

What classification code is assigned to this device?

This device is registered under product classification code L159099.

Programmatic Export

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

JSON API Endpoint