Pomee (UDI 702-292)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pomee (Model/Catalog Number: 702-292) is a medical device manufactured by POMEE CORPORATION. This product is indexed under FDA Product Code / Category Classification EMK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 702-292
Product Code / EMDN: EMK
Device Name: Surgical Curettes Molt #2
Database Sync Date: 2026-08-09 09:04:00

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 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 702-292.

What classification code is assigned to this device?

This device is registered under product classification code EMK.

Similar Classification Devices (EMK)

Other Devices by POMEE CORPORATION

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