gudid
Primary ID: PAPS2
Penumbra System (UDI PAPS2)
Manufactured by PENUMBRA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Penumbra System - Primary ID PAPS2
Device Regulatory Overview
The Penumbra System (Model/Catalog Number: PAPS2) is a medical device manufactured by PENUMBRA, INC.. This product is indexed under FDA Product Code / Category Classification JCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PAPS2
- Product Code / EMDN
- JCX
- Device Name
- PS Pump Canister Kit
- Database Sync Date
- 2026-08-09 09:43:31
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 Penumbra System?
The registered manufacturer of record for Penumbra System is PENUMBRA, INC..
What is the Primary UDI-DI identifier for Penumbra System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PAPS2.
What classification code is assigned to this device?
This device is registered under product classification code JCX.
Similar Classification Devices (JCX)
Other Devices by PENUMBRA, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint