GUDIDData
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gudid Primary ID: RDA72-03

CONMED (UDI RDA72-03)

Manufactured by Conmed Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CONMED - Primary ID RDA72-03

Device Regulatory Overview

The CONMED (Model/Catalog Number: RDA72-03) is a medical device manufactured by Conmed Corporation. This product is indexed under FDA Product Code / Category Classification BZQ 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-2597-2016 View Full Alert →

Pediatric ThermoGard Dual Dispersive Electrodes (for patients 5-15 kg.), 10' (3.05m) Cable, Catalog Number 51-7710. Intended to be used f...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2599-2016 View Full Alert →

Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.), use with the Birtcher Pad Sensing System (PSS) on the Birtcher Systems 6000, 6...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2598-2016 View Full Alert →

Adult Dual Dispersive Electrodes (for patients >15 kg.), use with the Birtcher Pad Sensing System (PSS) on the Birtcher Systems 6000, 6400, ...

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

Technical Specifications

Model Number
RDA72-03
Product Code / EMDN
BZQ
Device Name
Unshielded, 72 Inch, 3 lead, snap connector
Database Sync Date
2026-08-09 09:17:29

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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Frequently Asked Questions

Who is the primary manufacturer of CONMED?

The registered manufacturer of record for CONMED is Conmed Corporation.

What is the Primary UDI-DI identifier for CONMED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RDA72-03.

What classification code is assigned to this device?

This device is registered under product classification code BZQ.

Similar Classification Devices (BZQ)

Other Devices by Conmed Corporation

Programmatic Export

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

JSON API Endpoint