Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008467060

FEI Number

3008467060

Entity Name

Meifu Medical Technology Suzhou Co., Ltd.

City/State/Country

Suzhou Jiangsu, CN

Establishment Address

Bldg. 2 & 4,No 81 Tuncun West Road, Tongli Town, Wujiang District, Suzhou Jiangsu 215216, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Meifu Medical Technology Suzhou Co., Ltd. (Owner Number: 10033029)

Owner / Operator Contact Address

Bldg. 2 & 4,No 81 Tuncun West Road,, Tongli Town, Wujiang District, Suzhou, CN-JS 215216, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Magnet Pad Magnet Drape Urinal Comfort Ring Plastic Urinal Lid Uri-Clip Plastic Forceps Specimen Container

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2012-02-29
FOB	Bedpan	General Hospital	Class 1	880.6730	2016-07-08
KTC	Bath, Sitz, Nonpowered	Physical Medicine	Class 1	890.5125	2016-12-21
KNX	Collector, Urine, (And Accessories) For Indwelling Catheter	Gastroenterology, Urology	Class 2	876.5250	2012-05-09
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2010-07-07
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2012-08-30
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2010-07-07
FNP	Urinal	General Hospital	Class 1	880.6730	2011-12-01
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2011-03-09
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2010-07-07
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2010-07-07
ILS	Adaptor, Hygiene	Physical Medicine	Class 1	890.5050	2016-07-08
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2010-07-07

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Meifu Medical Technology Suzhou 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
K791969	Medline Industries, Inc.	DYNACOR STERILE CLOSED SYS. DRAINAGE BAG	1979-11-05
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02
K830425	Maddak, Inc.	TOILET SEAT RAISED	1983-05-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

Similar Registrations

Registration Number	Establishment Name	Location
3016215282	MINDERA CORPORATION	Vista, CA, US
3021006167	KIMS MED CO., LTD.	Gwangju, KR
3022320321	ALIRA MEDICAL DEVICES LLC	Rancho Cucamonga, CA, US
3015225571	Merit Medical Asia Company Limited	Tsim Sha Tsui, HK
2183744	Isomedix Operations, Inc.	Minneapolis, MN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008467060. Last updated year: 2026. Please use registration number 3008467060 when referencing this establishment in official correspondence.