Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006686250

FEI Number

3006686250

Entity Name

Guangzhou Schauenburg-Truplast Hose Technology Ltd.

City/State/Country

Guangzhou Guangdong, CN

Establishment Address

No.6 Nanjiang 3rd Road, Nansha District., Guangzhou Guangdong 511462, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Molded Devices, Inc. (Owner Number: 10058611)

Owner / Operator Contact Address

740 W Knox Road, Tempe, AZ 85284, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Single Patient Breathing Tube Slimline Tubing Standard Tubing Clear Grey CPAP Tubing: Expandable and Collapsible Tubing Performance Tubing / CPAP Hose

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2022-12-16
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2022-12-16

Official Correspondent

No official correspondent registered.

US Agent Details

Samuel Brayton Business: Aptyx Email: sbrayton@aptyx.com Phone: (518) 6360303

Related Public Records

Same Entity

Molded Devices, Inc.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1223009	MDI East, Inc., dba Medefab	JAFFREY, NH, US
3015146495	MOLDED DEVICES, INC.	Tempe, AZ, US
8022265	GLOBALMED, INC.	TRENTON Ontario, CA
1321175	BATES INDUSTRIES	S Glens Falls, NY, US
3011324393	MEDICAL MURRAY, INC.	Charlotte, NC, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2026	Percussionaire Corporation	1	Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

Similar Registrations

Registration Number	Establishment Name	Location
3027221819	MAGNAMED MEDICAL TECHNOLOGY	Fort Lauderdale, FL, US
3011971979	HAMILTON CENTRAL EUROPE	Giarmata Timis, RO
3014766741	Hamilton Medical AG	Domat / Ems Graubunden, CH
3015277818	HANGZHOU WEIZE IMP & EXP CO., LTD	Hangzhou Zhejiang, CN
3008281139	DANYANG XINYA VALVE CO., LTD.	Danyang Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006686250. Last updated year: 2026. Please use registration number 3006686250 when referencing this establishment in official correspondence.