GUDIDData
gudid Primary ID: 706-328

Pomee (UDI 706-328)

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 706-328

Device Regulatory Overview

The Pomee (Model/Catalog Number: 706-328) 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
706-328
Product Code / EMDN
EMH
Device Name
Extracting Forceps Universal Molar PX328
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
}
                            

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 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 706-328.

What classification code is assigned to this device?

This device is registered under product classification code EMH.

Programmatic Export

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

JSON API Endpoint