Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009498548

FEI Number

3009498548

Entity Name

NINGBO CAREMED MEDICAL PRODUCTS CO LTD

City/State/Country

Ningbo Zhejiang, CN

Establishment Address

No 79 Jiutang Rd, South side, Hangzhou Bay New Zone, Ningbo Zhejiang 315336, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

NINGBO CAREMED MEDICAL PRODUCTS CO LTD (Owner Number: 10038943)

Owner / Operator Contact Address

No 79 Jiutang Rd, South side, Hangzhou Bay New Zone, Ningbo, CN-ZJ 315336, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Medeco Plastcare USA Medline pen needle Lite touch Easy Glide Medtfine PIP JJ CARE Insulin Pen Needle LivaClean Health Insulin Pen Needle MedtLite Medt Medt - Fine Insulin Pen Needle Plastcare USA ADVOCATE ULTILET

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DZM	Needle, Dental	Dental	Class 1	872.4730	2011-11-27
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2014-08-03
EIB	Syringe, Irrigating (Dental)	Dental	Class 1	872.4565	2016-11-28
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2011-11-27

Official Correspondent

No official correspondent registered.

US Agent Details

LI QIAN Business: Carelife USA Inc. Email: li@carelifeusa.com Phone: (707) 9356499

Related Public Records

Same Entity

NINGBO CAREMED MEDICAL PRODUCTS 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
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

Similar Registrations

Registration Number	Establishment Name	Location
3005416271	C-K DENTAL IND. CO., LTD.	BUCHEON-SI, GYEONGGI-DO, KR
9612124	AIR WATER REALIZE INC.	IWAKI-SHI Fukushima, JP
3000247873	NIPRO CORPORATION	Settsu Osaka, JP
2416455	COLTENE/WHALEDENT INC.	CUYAHOGA FALLS, OH, US
9611446	NIPRO MEDICAL INDUSTRIES LTD.	TATEBAYASHI-SHI Gunma, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009498548. Last updated year: 2026. Please use registration number 3009498548 when referencing this establishment in official correspondence.