Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004527595

FEI Number

3004527595

Entity Name

QINGDAO TRAWORKS CO., LTD.

City/State/Country

QINGDAO Shandong, CN

Establishment Address

15 Donghai Road West, Inter Royal Building 16G, QINGDAO Shandong 266071, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Qingdao TraWorks Co., Ltd (Owner Number: 9072957)

Owner / Operator Contact Address

15 A DONGHAI ROAD West,, Inter Royal Building 16G, QINGDAO, CN-SD 266071, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Specimen Container LARYNGEAL MASK AIRWAY(LMA) STETHOSCOPES Nasopharyngeal Tube Intubating Stylet Urine Collector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2009-07-31
CAE	Airway, Oropharyngeal, Anesthesiology	Anesthesiology	Class 1	868.5110	2005-05-10
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2006-03-27
BTQ	Airway, Nasopharyngeal	Anesthesiology	Class 1	868.5100	2016-08-17
BSR	Stylet, Tracheal Tube	Anesthesiology	Class 1	868.5790	2016-07-18
NZU	Collector, Urine, Powered, Non Indwelling Catheter	Gastroenterology, Urology	Class 1	876.5250	2009-07-31

Official Correspondent

No official correspondent registered.

US Agent Details

Richard Manson Business: SOURCEMARK LLC Email: rmanson@sourcemarkusa.com Phone: (615) 2696010

Related Public Records

Same Entity

Qingdao TraWorks Co., Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2014	King Systems Corp.	1	King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004527595. Last updated year: 2026. Please use registration number 3004527595 when referencing this establishment in official correspondence.