Facility

NINGBO BESMED MEDICAL EQUIPMENT CORP.

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)	3006547005
Establishment type	Manufacture Medical Device
Location	NO.51, MO GAN SHAN RD, BEILUN NINGBO Zhejiang, CN 31580
Registration status	Active · expires 2026
Parent company	BESMED HEALTH BUSINESS CORP. (owner-operator 9047866)
Brand names	BESMED OXYGEN TUBING

Activity by year

Recalls (1)

Devices registered here (1)

Tubing, Pressure And Accessories
Product code BYX (opens in a new tab) · Class I · Anesthesiology · 21 CFR 868.5860

Recalls & enforcement

Class IITerminated2018-08-09
Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked AuraStraight Silicone, Single Use Laryngeal Mask Sterile

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. “NINGBO BESMED MEDICAL EQUIPMENT CORP. (FEI 3006547005) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006547005-ningbo-besmed-medical-equipment-corp/

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