GUDIDData
eudamed_udi Primary ID: 05033241031682

Surgical Suction Probe - Male Suction Probe (UDI 05033241031682)

Manufactured by Ivor Shaw Ltd trading as Pennine Healthcare

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Surgical Suction Probe - Male Suction Probe - Primary ID 05033241031682

Device Regulatory Overview

The Surgical Suction Probe - Male Suction Probe (Model/Catalog Number: SP-3800) is a medical device manufactured by Ivor Shaw Ltd trading as Pennine Healthcare. This product is indexed under FDA Product Code / Category Classification A06010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SP-3800
Product Code / EMDN
A06010103
Device Name
Surgical Suction Probes
Database Sync Date
2026-08-09 16:28:47

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 Surgical Suction Probe - Male Suction Probe?

The registered manufacturer of record for Surgical Suction Probe - Male Suction Probe is Ivor Shaw Ltd trading as Pennine Healthcare.

What is the Primary UDI-DI identifier for Surgical Suction Probe - Male Suction Probe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05033241031682.

What classification code is assigned to this device?

This device is registered under product classification code A06010103.

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