GUDIDData
gudid Primary ID: SK-950C

Perimeter (UDI SK-950C)

Manufactured by CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perimeter - Primary ID SK-950C

Device Regulatory Overview

The Perimeter (Model/Catalog Number: SK-950C) is a medical device manufactured by CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD. This product is indexed under FDA Product Code / Category Classification HPT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SK-950C
Product Code / EMDN
HPT
Device Name
It is an AC-powered or manual device intended to determine the extent of the peripheral visual field of a patient. The device projects light on various points of a curved surface, and the patient indicates whether he or she sees the light
Database Sync Date
2026-08-09 09:06:39

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Perimeter?

The registered manufacturer of record for Perimeter is CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD.

What is the Primary UDI-DI identifier for Perimeter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SK-950C.

What classification code is assigned to this device?

This device is registered under product classification code HPT.

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