Facility

Hangzhou Bever Medical Devices Co., Ltd.

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3008729910
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	Building 2, No. 1-1, Houmuqiao Hangzhou Zhejiang, CN 31112
Registration status	Active · expires 2026
Parent company	Hangzhou Bever Medical Devices Co., Ltd. (owner-operator 10034111)
Brand names	BD Intermittent Catheter; Intermittent Catheter

Activity by year

Recalls (1)

Devices registered here (1)

Catheter, Urethral
Product code GBM (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5130

Recalls & enforcement

Class IIOngoing2025-11-29
Labeling error, Incorrect expiration date

All facilities operated by Hangzhou Bever Medical Devices Co., Ltd.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Hangzhou Bever Medical Devices Co., Ltd. (FEI 3008729910) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008729910-hangzhou-bever-medical-devices-co-ltd/

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