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emdn_classification Primary ID: Z12062880

NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES (UDI Z12062880)

Manufactured by

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES - Primary ID Z12062880

Device Regulatory Overview

The NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification Z12062880 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-2753-2026 View Full Alert →

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Technical Specifications

Model Number
N/A
Product Code / EMDN
Z12062880
Device Name
NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES
Database Sync Date
2026-08-09 16:18:37

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 NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES?

The registered manufacturer of record for NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES is .

What is the Primary UDI-DI identifier for NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z12062880.

What classification code is assigned to this device?

This device is registered under product classification code Z12062880.

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