GUDIDData
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eudamed_udi Primary ID: 00884838089655

E/R Temp Probe 12 FR Reuse Autoclavable (UDI 00884838089655)

Manufactured by Philips Medical Systems

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for E/R Temp Probe 12 FR Reuse Autoclavable - Primary ID 00884838089655

Device Regulatory Overview

The E/R Temp Probe 12 FR Reuse Autoclavable (Model/Catalog Number: 989803203561) is a medical device manufactured by Philips Medical Systems. This product is indexed under FDA Product Code / Category Classification Z1203020201 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-0745-2016 View Full Alert →

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ID: Z-0010-2017 View Full Alert →

Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body...

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ID: Z-0012-2017 View Full Alert →

Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body...

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

Technical Specifications

Model Number
989803203561
Product Code / EMDN
Z1203020201
Device Name
Temperature Probes, Reusable
Database Sync Date
2026-08-09 16:51:07

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 E/R Temp Probe 12 FR Reuse Autoclavable?

The registered manufacturer of record for E/R Temp Probe 12 FR Reuse Autoclavable is Philips Medical Systems.

What is the Primary UDI-DI identifier for E/R Temp Probe 12 FR Reuse Autoclavable?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838089655.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020201.

Similar Classification Devices (Z1203020201)

Other Devices by Philips Medical Systems

Programmatic Export

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