gudid Primary ID: N/a

Amnicators (UDI N/a)

Manufactured by MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Amnicators (Model/Catalog Number: N/a) is a medical device manufactured by MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED. This product is indexed under FDA Product Code / Category Classification HIO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/a
Product Code / EMDN: HIO
Device Name: Amniotic Fluid Indicator
Database Sync Date: 2026-08-09 09:57:34

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Amnicators?

The registered manufacturer of record for Amnicators is MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED.

What is the Primary UDI-DI identifier for Amnicators?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N/a.

What classification code is assigned to this device?

This device is registered under product classification code HIO.

Similar Classification Devices (HIO)

Other Devices by MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint