GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 00884838125223

Portable Panel Protector (UDI 00884838125223)

Manufactured by Philips Medical Systems DMC GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Portable Panel Protector - Primary ID 00884838125223

Device Regulatory Overview

The Portable Panel Protector (Model/Catalog Number: 989701000994) is a medical device manufactured by Philips Medical Systems DMC GmbH. This product is indexed under FDA Product Code / Category Classification Z11039080 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0466-2026 View Full Alert →

Radiography 7300 C; Model Number: 712037;...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1327-2022 View Full Alert →

DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1325-2022 View Full Alert →

ProxiDiagnost N90. radiography and fluoroscopy system...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
989701000994
Product Code / EMDN
Z11039080
Device Name
Detector Accessory
Database Sync Date
2026-08-09 17:13:06

Full Regulatory Attributes

🔒 Token Gated 
{
    "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 Portable Panel Protector?

The registered manufacturer of record for Portable Panel Protector is Philips Medical Systems DMC GmbH.

What is the Primary UDI-DI identifier for Portable Panel Protector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838125223.

What classification code is assigned to this device?

This device is registered under product classification code Z11039080.

Similar Classification Devices (Z11039080)

Other Devices by Philips Medical Systems DMC GmbH

Programmatic Export

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

JSON API Endpoint