GUDIDData
eudamed_udi Primary ID: E1652520021

roeko-Swab/hazelnut, 500 pcs. (UDI E1652520021)

Manufactured by Coltène/Whaledent GmbH + Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for roeko-Swab/hazelnut, 500 pcs. - Primary ID E1652520021

Device Regulatory Overview

The roeko-Swab/hazelnut, 500 pcs. (Model/Catalog Number: 252002) is a medical device manufactured by Coltène/Whaledent GmbH + Co. KG. This product is indexed under FDA Product Code / Category Classification M020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
252002
Product Code / EMDN
M020199
Device Name
roeko-Swab non-sterile
Database Sync Date
2026-08-09 16:28:50

Full Regulatory Attributes

🔒 Token Gated
{
    "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 roeko-Swab/hazelnut, 500 pcs.?

The registered manufacturer of record for roeko-Swab/hazelnut, 500 pcs. is Coltène/Whaledent GmbH + Co. KG.

What is the Primary UDI-DI identifier for roeko-Swab/hazelnut, 500 pcs.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E1652520021.

What classification code is assigned to this device?

This device is registered under product classification code M020199.

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