Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038624873

FEI Number

3038624873

Entity Name

RUIAN SUNNYWORLD INTERNATIONAL TRADE CO.,LTD

City/State/Country

RUIAN Zhejiang, CN

Establishment Address

XIN CHAO BUILDING A-702, LONG SHAN EAST ROAD, RUIAN Zhejiang 325200, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RUIAN SUNNYWORLD INTERNATIONAL TRADE CO.,LTD (Owner Number: 10093514)

Owner / Operator Contact Address

XIN CHAO BUILDING A-702, LONG SHAN EAST ROAD, RUIAN, CN-ZJ 325200, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Reflex Hammer Ophthalmoscope Otoscope Face Mask VENIPUNCTURE TRAINER injection training arm Simulation training model Stethoscope Pressure gauge Tourniquet PERCUSSOR Penlight MONOFILAMENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GWZ	Percussor	Neurology	Class 1	882.1700	2025-05-28
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2025-05-28
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2025-05-28
IQG	Adaptor, Holder, Syringe	Physical Medicine	Class 1	890.5050	2026-01-14
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2025-05-28
BXH	Gauge, Gas Pressure, Cylinder/Pipeline	Anesthesiology	Class 1	868.2610	2025-05-28
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2025-05-28
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2025-05-28
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2025-05-28
GXB	Esthesiometer	Neurology	Class 1	882.1500	2026-04-02

Official Correspondent

Manny Chen

US Agent Details

Creekon Yang Business: SPICA MEDTECH CORP Email: fda.agent@spicagloble.com Phone: (720) 6176666

Related Public Records

Same Entity

RUIAN SUNNYWORLD INTERNATIONAL TRADE CO.,LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

Similar Registrations

Registration Number	Establishment Name	Location
9710524	ULTIMATE MEDICAL PRODUCTS LTD.	SHARJAH Ash Shariqah, AE
3003418325	Integra LifeSciences Corporation	Princeton, NJ, US
9611283	DIMEDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE
3035708926	MED2B LTD.	Kitzingen Bavaria, DE
3005809810	Jarit GmbH	Rietheim-Weilheim Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038624873. Last updated year: 2026. Please use registration number 3038624873 when referencing this establishment in official correspondence.