eudamed_udi Primary ID: 00816995021230

Kit, VHP, Nose Cone and O-Rings, Vaser (UDI 00816995021230)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Kit, VHP, Nose Cone and O-Rings, Vaser (Model/Catalog Number: 130-0170) is a medical device manufactured by Solta Medical, Inc.. This product is indexed under FDA Product Code / Category Classification L250399 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1463-2014 View Full Alert →

FRAXEL DUAL 1550/1927 Laser System, (FRAXEL SR 1500 DUAL Laser System), for dermatological procedures....

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Technical Specifications

Model Number: 130-0170
Product Code / EMDN: L250399
Device Name: PROBE, PACKAGED, 2.9MM, 11CM, 3-GROOVE
Database Sync Date: 2026-08-09 18:32:23

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 Kit, VHP, Nose Cone and O-Rings, Vaser?

The registered manufacturer of record for Kit, VHP, Nose Cone and O-Rings, Vaser is Solta Medical, Inc..

What is the Primary UDI-DI identifier for Kit, VHP, Nose Cone and O-Rings, Vaser?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00816995021230.

What classification code is assigned to this device?

This device is registered under product classification code L250399.

Similar Classification Devices (L250399)

Other Devices by Solta Medical, Inc.

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