GUDIDData
eudamed_udi Primary ID: 05060031473940

Eclypse Adherent Sacral (UDI 05060031473940)

Manufactured by Brightwake Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eclypse Adherent Sacral - Primary ID 05060031473940

Device Regulatory Overview

The Eclypse Adherent Sacral (Model/Catalog Number: CR3985) is a medical device manufactured by Brightwake Limited. This product is indexed under FDA Product Code / Category Classification M040204 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CR3985
Product Code / EMDN
M040204
Device Name
Eclypse Adherent Sacral
Database Sync Date
2026-08-09 16:45:00

Full Regulatory Attributes

๐Ÿ”’ 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 Eclypse Adherent Sacral?

The registered manufacturer of record for Eclypse Adherent Sacral is Brightwake Limited.

What is the Primary UDI-DI identifier for Eclypse Adherent Sacral?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060031473940.

What classification code is assigned to this device?

This device is registered under product classification code M040204.

Programmatic Export

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

JSON API Endpoint