GUDIDData
classification Primary ID: SDV

Clinical Electronic Thermometer (UDI SDV)

Manufactured by

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Clinical Electronic Thermometer - Primary ID SDV

Device Regulatory Overview

The Clinical Electronic Thermometer (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification SDV 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-2753-2026 View Full Alert →

FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2755-2026 View Full Alert →

FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, I...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2793-2026 View Full Alert →

SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System...

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

Technical Specifications

Model Number
N/A
Product Code / EMDN
SDV
Device Name
Clinical Electronic Thermometer
Database Sync Date
2026-08-09 09:00:27

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 Clinical Electronic Thermometer?

The registered manufacturer of record for Clinical Electronic Thermometer is .

What is the Primary UDI-DI identifier for Clinical Electronic Thermometer?

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

What classification code is assigned to this device?

This device is registered under product classification code SDV.

Programmatic Export

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

JSON API Endpoint