gudid Primary ID: GoodKnight 420G

GoodKnight (UDI GoodKnight 420G)

Manufactured by SEFAM

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

Scannable UDI-DI Representation

Device Regulatory Overview

The GoodKnight (Model/Catalog Number: GoodKnight 420G) is a medical device manufactured by SEFAM. This product is indexed under FDA Product Code / Category Classification BZD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: GoodKnight 420G
Product Code / EMDN: BZD
Device Name: GoodKnight 420G is a basic sleep apnea therapy device (PAP device).
Database Sync Date: 2026-08-09 09:52:14

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 GoodKnight?

The registered manufacturer of record for GoodKnight is SEFAM.

What is the Primary UDI-DI identifier for GoodKnight?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GoodKnight 420G.

What classification code is assigned to this device?

This device is registered under product classification code BZD.

Similar Classification Devices (BZD)

Other Devices by SEFAM

Programmatic Export

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

JSON API Endpoint