GUDIDData
gudid Primary ID: 711-045

Pomee (UDI 711-045)

Manufactured by POMEE CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pomee - Primary ID 711-045

Device Regulatory Overview

The Pomee (Model/Catalog Number: 711-045) is a medical device manufactured by POMEE CORPORATION. This product is indexed under FDA Product Code / Category Classification EMH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
711-045
Product Code / EMDN
EMH
Device Name
Blumenthal 6" 45 degree tip
Database Sync Date
2026-08-09 09:04:00

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 Pomee?

The registered manufacturer of record for Pomee is POMEE CORPORATION.

What is the Primary UDI-DI identifier for Pomee?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 711-045.

What classification code is assigned to this device?

This device is registered under product classification code EMH.

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