gudid
Primary ID: 0600-MG3012-000
Laser Lavage MG (UDI 0600-MG3012-000)
Manufactured by MECTRA LABS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Laser Lavage MG - Primary ID 0600-MG3012-000
Device Regulatory Overview
The Laser Lavage MG (Model/Catalog Number: 0600-MG3012-000) is a medical device manufactured by MECTRA LABS, INC.. This product is indexed under FDA Product Code / Category Classification GBX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0600-MG3012-000
- Product Code / EMDN
- GBX
- Device Name
- Laser Lavage MG Dual Spike
- Database Sync Date
- 2026-08-09 09:32:55
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Laser Lavage MG?
The registered manufacturer of record for Laser Lavage MG is MECTRA LABS, INC..
What is the Primary UDI-DI identifier for Laser Lavage MG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0600-MG3012-000.
What classification code is assigned to this device?
This device is registered under product classification code GBX.
Similar Classification Devices (GBX)
Other Devices by MECTRA LABS, INC.
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