Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005855942

FEI Number

3005855942

Entity Name

GVS Technology (Suzhou) Co., Ltd

City/State/Country

Suzhou Jiangsu, CN

Establishment Address

No.8 Taishan Road, Suzhou New District SND, Suzhou Jiangsu 215129, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

GVS Technology (Suzhou) Co., Ltd (Owner Number: 10032971)

Owner / Operator Contact Address

No.8 Taishan Road, Suzhou New District SND, Suzhou, CN-JS 215129, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

9085/M/751 8866/M/750 9080/M/750 9064/M/751 9065/750+a620/60/61 9067/M/750 4333/M/752 DYNJAAHME14 9500/710 DYNJAAHME14-B 9064/751+a620/60/61 9066/M/751 4333/M/751 9065/M/750 9064/M/752 9064/750 9065/750 9085/751 9064/751 4333/750 9066/751 8866/50 4333/752 4333/751 9080/750 9067/750 9066/750 4333/754 1600 2800 100 PFT filters CO2 Absorber 1898/711KBSBB

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYD	Condenser, Heat And Moisture (Artificial Nose)	Anesthesiology	Class 1	868.5375	2011-12-14
BZG	Spirometer, Diagnostic	Anesthesiology	Class 2	868.1840	2011-01-17
BSF	Absorber, Carbon-Dioxide	Anesthesiology	Class 1	868.5310	2020-12-15

Official Correspondent

No official correspondent registered.

US Agent Details

Matt Dryden Business: ProMedic, LLC Email: matt.dryden@promedic.cc Phone: (239) 3076063

Related Public Records

Same Entity

GVS Technology (Suzhou) 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
K923989	Sensor Medics Corp.	SENSORMEDICS MODEL 6200 AUTOBOX DL	1993-08-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0006-2008	Datex Ohmeda, Inc	1	GE Disposable Multi Absorber Canister used with EZchange Module for the Aisys, Avance, Aespire Anesthesia systems. The EZchange Module is an optional accessory for these anesthesia systems.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005855942. Last updated year: 2026. Please use registration number 3005855942 when referencing this establishment in official correspondence.