gudid Primary ID: PinPoint chamber 0.015 cm

PinPoint (UDI PinPoint chamber 0.015 cm)

Manufactured by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The PinPoint (Model/Catalog Number: PinPoint chamber 0.015 cm) is a medical device manufactured by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH. This product is indexed under FDA Product Code / Category Classification LHN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PinPoint chamber 0.015 cm
Product Code / EMDN: LHN
Device Name
Database Sync Date: 2026-08-09 09:51:22

Full Regulatory Attributes

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{
    "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 PinPoint?

The registered manufacturer of record for PinPoint is PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH.

What is the Primary UDI-DI identifier for PinPoint?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PinPoint chamber 0.015 cm.

What classification code is assigned to this device?

This device is registered under product classification code LHN.

Similar Classification Devices (LHN)

Other Devices by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH

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