BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.

FDA Device Registration & Listing · Beijing, CN · Registration 3008191276

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
3008191276
FEI Number
3008191276
Entity Name
BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.
City/State/Country
Beijing, CN
Establishment Address
Building 5, No. 8, Yanqi West Road, Yanqi Economic Development Zone, Huairou District, Beijing 101407, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Beijing Ruicheng Medical Supplies Co., Ltd. (Owner Number: 10031145)
Owner / Operator Contact Address
Building 5, No. 8, Yanqi West Road, Yanqi Economic Development Zone, Huairou District, Beijing, CN-BJ 101407, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Lancet Simple Diagnostics Lancet Device Pharmacist Choice Lancets Simple Diagnostics Lancets DS-W Pharmacist Choice Lancet Device CareSens Lancing device Tempo Lancing device CareSoft Lancing Device Lancing device RC-LD-21 DS-A Clever Choice Lancet Device Lite Lancing Device Clever Choice Lancets Alcohol Prep Pad Clever Choice Alcohol Prep Pads Pharmacist Choice Alcohol Prep Pads Simple Diagnostics Alcohol Prep Pads LD4300 LD2111 Hemovista Safety Lancet LD3300 Disposable Safety Aktivsafe Lancet (TD- 5083) Disposable Safety Lancet Disposable Safety Blade Lancet E1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QRL Multiple Use Blood Lancet For Single Patient Use Only General, Plastic Surgery Class 2 878.4850 2022-09-26
QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2022-09-26
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2009-12-23
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2022-12-05

Official Correspondent

yuechao li

US Agent Details

James H. Liao Email: james@sino2us.com Phone: (310) 3758169

Related Public Records

Same Entity

Beijing Ruicheng Medical Supplies 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
K130132 Medipurpose Pte. , Ltd. BABYLANCE HEEL INCISION DEVICE 2013-02-11

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0044-2008 Becton Dickinson & Company 2
Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008191276. Last updated year: 2026. Please use registration number 3008191276 when referencing this establishment in official correspondence.
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