gudid
Primary ID: 713-301
Pomee (UDI 713-301)
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 713-301
Device Regulatory Overview
The Pomee (Model/Catalog Number: 713-301) is a medical device manufactured by POMEE CORPORATION. This product is indexed under FDA Product Code / Category Classification EIK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 713-301
- Product Code / EMDN
- EIK
- Device Name
- PK THOMAS WAX #1
- 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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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 713-301.
What classification code is assigned to this device?
This device is registered under product classification code EIK.
Similar Classification Devices (EIK)
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