DU-HOPE INTERNATIONAL GROUP

FDA Device Registration & Listing · NANJING Jiangsu, CN · Registration 8043965

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
8043965
FEI Number
3010491498
Entity Name
DU-HOPE INTERNATIONAL GROUP
City/State/Country
NANJING Jiangsu, CN
Establishment Address
199 JIANYE ROAD, NANJING Jiangsu --, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DU-HOPE INTERNATIONAL GROUP (Owner Number: 9004860)
Owner / Operator Contact Address
199 JIANYE ROAD, --, NANJING, CN-NOTA --, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

invalid ring sanitary belt bathroom thermometer eye shield ice cap urinal bottle ear syringe hot water bottle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2008-06-23
ISR Band Or Belt, Pelvic Support Physical Medicine Class 1 890.3025 2011-08-31
FLK Thermometer, Clinical Mercury General Hospital Class 2 880.2920 1993-03-04
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2003-11-04
KYR Bag, Ice General Hospital Class 1 880.6050 2003-11-04
FNP Urinal General Hospital Class 1 880.6730 2004-10-18
JZF Tube, Ear Suction Ear, Nose, Throat Class 1 874.4420 2008-06-23
FPF Bottle, Hot/Cold Water General Hospital Class 1 880.6085 1993-03-04

Official Correspondent

MIKE GUAN

US Agent Details

Mike Ming Guan Email: mmguan.newland@gmail.com Phone: (714) 3067531

Related Public Records

Same Entity

DU-HOPE INTERNATIONAL GROUP
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043965. Last updated year: 2026. Please use registration number 8043965 when referencing this establishment in official correspondence.
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