eudamed_udi Primary ID: ++G231DE12621264

WEITLANER 10.5CM (UDI ++G231DE12621264)

Manufactured by RAJ IMPEX

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

Scannable UDI-DI Representation

Device Regulatory Overview

The WEITLANER 10.5CM (Model/Catalog Number: DE-1262-1264) is a medical device manufactured by RAJ IMPEX. This product is indexed under FDA Product Code / Category Classification L150201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DE-1262-1264
Product Code / EMDN: L150201
Device Name: WEITLANER 10.5CM
Database Sync Date: 2026-08-09 16:51:30

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of WEITLANER 10.5CM?

The registered manufacturer of record for WEITLANER 10.5CM is RAJ IMPEX.

What is the Primary UDI-DI identifier for WEITLANER 10.5CM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ++G231DE12621264.

What classification code is assigned to this device?

This device is registered under product classification code L150201.

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