NINGBO BEIERXIN BABY ACCESSORIES CO., LTD.

FDA Device Registration & Listing · Ningbo Zhejiang, CN · Registration 3012030719

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012030719
FEI Number
3012030719
Entity Name
NINGBO BEIERXIN BABY ACCESSORIES CO., LTD.
City/State/Country
Ningbo Zhejiang, CN
Establishment Address
No.1, Jishan Village, Xidian Town, Ninghai County, Ningbo Zhejiang 315613, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ningbo Beierxin Baby Accessories Co., Ltd. (Owner Number: 10089461)
Owner / Operator Contact Address
No.1, Jishan Village, Xidian Town, Ninghai County, Ningbo, CN-ZJ 315613, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

toothbrush Nasal aspirator MEDICAL DROPPER PERI BOTTLE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFW Toothbrush, Manual Dental Class 1 872.6855 2025-02-04
BSY Catheters, Suction, Tracheobronchial Anesthesiology Class 1 868.6810 2023-12-11
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2023-12-11
HED Douche Apparatus, Vaginal, Therapeutic Obstetrics/Gynecology Class 1 884.5900 2023-12-10

Official Correspondent

Isabella Luo

US Agent Details

Rae Zhang Email: Rae@ashtelstudios.com Phone: (909) 4340911

Related Public Records

Same Entity

Ningbo Beierxin Baby Accessories 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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012030719. Last updated year: 2026. Please use registration number 3012030719 when referencing this establishment in official correspondence.
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