GUDIDData
gudid Primary ID: 40-0531HFDLC

PA TUNNELING INSTRUMENT #2 D/E DLC HF HANDLE (UDI 40-0531HFDLC)

Manufactured by W.H. Holden, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PA TUNNELING INSTRUMENT #2 D/E DLC HF HANDLE - Primary ID 40-0531HFDLC

Device Regulatory Overview

The PA TUNNELING INSTRUMENT #2 D/E DLC HF HANDLE (Model/Catalog Number: 40-0531HFDLC) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification EMO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
40-0531HFDLC
Product Code / EMDN
EMO
Device Name
Database Sync Date
2026-08-09 09:01:14

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 PA TUNNELING INSTRUMENT #2 D/E DLC HF HANDLE?

The registered manufacturer of record for PA TUNNELING INSTRUMENT #2 D/E DLC HF HANDLE is W.H. Holden, Inc..

What is the Primary UDI-DI identifier for PA TUNNELING INSTRUMENT #2 D/E DLC HF HANDLE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 40-0531HFDLC.

What classification code is assigned to this device?

This device is registered under product classification code EMO.

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