Ningbo Haishu Zonghai Artware Co., Ltd.

FDA Device Registration & Listing · Ningbo City Zhejiang, CN · Registration 3009694272

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
3009694272
FEI Number
3009694272
Entity Name
Ningbo Haishu Zonghai Artware Co., Ltd.
City/State/Country
Ningbo City Zhejiang, CN
Establishment Address
Guangsheng Village, Jishigang Town, Haishu District, Ningbo City Zhejiang 315172, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ningbo Haishu Zonghai Artware Co., Ltd. (Owner Number: 10041107)
Owner / Operator Contact Address
Guangsheng Village, Jishigang Town, Haishu District, Ningbo City, CN-ZJ 315172, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Pill Splitter ECONOMY PILL SPLITTER - RAW ECONOMY PILL SPLITTER CHROME ULTRA GRIP BATH HANDLE 12" INDICATOR FOR SECURITY ULTRA GRIP BATH HANDLE 12” ULTRA GRIP BAR XTRA 16” Plastic Bath Suction Handle ULTRA GRIP PIVOT 19” MUTI POSITION GRABBER Contact Lens Case

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHY Pill Crusher/Cutter General Hospital Class 1 880.6430 2012-06-20
IKX Aid, Transfer Physical Medicine Class 1 890.5050 2012-06-20
ILS Adaptor, Hygiene Physical Medicine Class 1 890.5050 2016-12-06
LRX Case, Contact Lens Ophthalmic Class 2 886.5928 2016-12-14

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Ningbo Haishu Zonghai Artware 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
K830425 Maddak, Inc. TOILET SEAT RAISED 1983-05-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009694272. Last updated year: 2026. Please use registration number 3009694272 when referencing this establishment in official correspondence.
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