GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 04055207041130

Unspecified Brand (UDI 04055207041130)

Manufactured by Richard Wolf GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04055207041130

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 8083.001) is a medical device manufactured by Richard Wolf GmbH. This product is indexed under FDA Product Code / Category Classification L060403 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-1753-2025 View Full Alert →

PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoe...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1868-2018 View Full Alert →

RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2897-2018 View Full Alert →

Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgica...

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

Technical Specifications

Model Number
8083.001
Product Code / EMDN
L060403
Device Name
Modular handles, non HF
Database Sync Date
2026-08-09 16:46:06

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Richard Wolf GmbH.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04055207041130.

What classification code is assigned to this device?

This device is registered under product classification code L060403.

Similar Classification Devices (L060403)

Other Devices by Richard Wolf GmbH

Programmatic Export

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

JSON API Endpoint