BEIJING KINGST COMMERCIAL & TRADE CO., LTD.

FDA Device Registration & Listing · Beijing, CN · Registration 3012733231

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
3012733231
FEI Number
3012733231
Entity Name
BEIJING KINGST COMMERCIAL & TRADE CO., LTD.
City/State/Country
Beijing, CN
Establishment Address
5/F, Building 3, No.27, Yongwang Road, Z-park Daxing Bio-medicine Industry Park, Dist. Daxing, Beijing 102600, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Beijing Kingst Commercial & Trade Co., Ltd. (Owner Number: 10053621)
Owner / Operator Contact Address
5/F, Building 3, No.27, Yongwang Road, Z-park Daxing Bio-medicine Industry Park, Dist. Daxing, Beijing, CN-BJ 102600, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

VPOD CapOx PC-900B Capno-H Capnograph and Oximeter HLS CORE CO2 Sidestream Module Capno-S, Capno-S+,CapnoCore2 CO2 Sidestream Sensor KM7002 CO2 Mainstream Sensor CO2 Mainstream Module Capno-M, Capno-M+

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase Anesthesiology Class 2 868.1400 2018-07-30
DQA Oximeter Cardiovascular Class 2 870.2700 2018-07-30
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase Anesthesiology Class 2 868.1400 2020-05-25
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase Anesthesiology Class 2 868.1400 2020-05-25

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Beijing Kingst Commercial & Trade 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
K142467 Abeon Medical Corporation IntelAir Nasal Airway Support System 2014-11-24
K861213 Datex Division Instrumentarium Corp. PB 254 IR - SPECTROMETER 1986-04-04
K172904 Philips Medizin Systeme Boeblingen GmbH IntelliVue Capnography Extension, IntelliVue Microstream Extension 2017-12-26
K903523 Hewlett-Packard Co. HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE 1990-10-23
K973147 Nellcor Puritan Bennett, Inc. NPB-295 PULSE OXIMETER 1997-11-14

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0021-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N, Part Number CS08651-01
Z-0024-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657
Z-0025-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02
Z-0026-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N W/PRINTER, Part Number CS08657-01
Z-0027-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-03

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3010427901 CMI Health, Inc. Alpharetta, GA, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012733231. Last updated year: 2026. Please use registration number 3012733231 when referencing this establishment in official correspondence.
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