GUDIDData
eudamed_udi Primary ID: 08006530010610

blend-a-dent (UDI 08006530010610)

Manufactured by Procter & Gamble Technical Centres Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for blend-a-dent - Primary ID 08006530010610

Device Regulatory Overview

The blend-a-dent (Model/Catalog Number: 80896819) is a medical device manufactured by Procter & Gamble Technical Centres Limited. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
80896819
Product Code / EMDN
Q010280
Device Name
Denture Adhesive
Database Sync Date
2026-08-09 16:50:54

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 blend-a-dent?

The registered manufacturer of record for blend-a-dent is Procter & Gamble Technical Centres Limited.

What is the Primary UDI-DI identifier for blend-a-dent?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08006530010610.

What classification code is assigned to this device?

This device is registered under product classification code Q010280.

Programmatic Export

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

JSON API Endpoint