Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008729910

FEI Number

3008729910

Entity Name

Hangzhou Bever Medical Devices Co., Ltd.

City/State/Country

Hangzhou Zhejiang, CN

Establishment Address

Building 2, No. 1-1, Houmuqiao, Yongle Village, Cangqian Street, Yuhang District, Hangzhou Zhejiang 311121, CN

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Hangzhou Bever Medical Devices Co., Ltd. (Owner Number: 10034111)

Owner / Operator Contact Address

Building 2, No. 1-1, Houmuqiao, Yongle Village,Cangqian St.,Yuhang Dist., Hangzhou, CN-ZJ 311121, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ready-to-Use Hydrophilic Catheter BD Ready-to-Use Hydrophilic Catheter BD Intermittent Catheter Intermittent Catheter Robertazzi Nasopharyngeal Airway Nasopharyngeal Airway

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GBM	Catheter, Urethral	Gastroenterology, Urology	Class 2	876.5130	2020-01-09
EZD	Catheter, Straight	Gastroenterology, Urology	Class 2	876.5130	2020-01-09
GBM	Catheter, Urethral	Gastroenterology, Urology	Class 2	876.5130	2012-02-17
BTQ	Airway, Nasopharyngeal	Anesthesiology	Class 1	868.5100	2010-11-05

Official Correspondent

Allyson Zhou

US Agent Details

Phoenix Wang Email: wcy_2@hotmail.com Phone: (405) 6945955

Related Public Records

Same Entity

Hangzhou Bever Medical Devices Co., Ltd.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0004-2013	Cure Medical LLC	2	Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in intermediate boxes containing 30 individual, sterile packaged catheters (PA/PE film and dialyzing paper pouches). There are 30 catheters packaged in sterile pouches that are placed into an intermediate box, 10 of these intermediate boxes packaged into one case. K072539 The Cure Catheter" device, M16, is an intermittent urinary catheter intended to be used by males for the purpose of bladder drainage. It is manufactured with conventional medical grade, latex-free, biocompatible materials. The straight-tip has been designed to eliminate trauma to the urethra and is provided in 16Fr size in an easy-to-open, sterile, single-use package. The coud-tip catheter, M16C, is designed with a curved tip that makes it easier to pass through the curvature of the prostatic urethra in men. It is also used to pass through urethral strictures. This product is prescribed for people who have difficulty or are unable to pass a straight catheter through their urethra and into their bladder.

Similar Registrations

Registration Number	Establishment Name	Location
9613662	MEDISCAN GMBH & CO. KG	KREMSMUNSTER Oberosterreich, AT
3008502431	HR PHARMACEUTICALS, INC d/b/a HR HealthCare	York, PA, US
1417592	MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, US
3006606901	COLOPLAST HUNGARY KFT	NYIRBATOR Szabolcs-Szatmar-Bereg, HU
3008806809	ConvaTec Limited, GDC Building	Deeside Flintshire, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008729910. Last updated year: 2026. Please use registration number 3008729910 when referencing this establishment in official correspondence.