eudamed_udi
Primary ID: 00866203000243
PEA POD (UDI 00866203000243)
Manufactured by COSMED USA, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PEA POD - Primary ID 00866203000243
Device Regulatory Overview
The PEA POD (Model/Catalog Number: PP2025) is a medical device manufactured by COSMED USA, Inc.. This product is indexed under FDA Product Code / Category Classification Z12159007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PP2025
- Product Code / EMDN
- Z12159007
- Device Name
- BOD POD & PEA POD
- Database Sync Date
- 2026-08-09 18:13:43
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 PEA POD?
The registered manufacturer of record for PEA POD is COSMED USA, Inc..
What is the Primary UDI-DI identifier for PEA POD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00866203000243.
What classification code is assigned to this device?
This device is registered under product classification code Z12159007.
Similar Classification Devices (Z12159007)
Other Devices by COSMED USA, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint