TESS BASE (UDI A1700380)

Manufactured by BIOMET

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

Scannable UDI-DI Representation

Device Regulatory Overview

The TESS BASE (Model/Catalog Number: A1700380) is a medical device manufactured by BIOMET. This product is indexed under FDA Product Code / Category Classification FSM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: A1700380
Product Code / EMDN: FSM
Device Name
Database Sync Date: 2026-08-09 09:23:29

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 TESS BASE?

The registered manufacturer of record for TESS BASE is BIOMET.

What is the Primary UDI-DI identifier for TESS BASE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A1700380.

What classification code is assigned to this device?

This device is registered under product classification code FSM.

Similar Classification Devices (FSM)

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