Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007417753

FEI Number

3007417753

Entity Name

MAQUET (SUZHOU) CO., LTD

City/State/Country

Suzhou Jiangsu, CN

Establishment Address

No.158, Fang Zhou Road, Suzhou Industrial Park, Suzhou Jiangsu 215024, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MAQUET (Suzhou) Co., Ltd (Owner Number: 10027696)

Owner / Operator Contact Address

No.158 Fang Zhou Road, SIP, Suzhou, CN-JS 215024, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Accessories to ALPHACLASSIC PRO, BETACLASSIC, MAQUET LYRA; YUNO; ALPHAMAXX; ALPHASTAR ; ALPHASTAR PRO; ALPHAMAQUET; BETASTAR; MEERA; MEERA CL; YUNO II Model: M-SHIFT ( including M-SHIFT Trolley ) Infusion Transfer System Model: MODUTEC (Including MODUTEC POWER, MODUTEC PLG II & MODUTEC SCREEN SOLUTION); M-CARRIER; M-LIFTING Medical Ceiling Supply Units Model: MODUEVO (including MODUEVO-MA, CARGOLIFT, ENERGY, PLG II, and MODUEVO BRIDGE) Acrobat

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BWN	Table And Attachments, Operating-Room	General, Plastic Surgery	Class 1	878.4950	2020-07-10
FOX	Stand, Infusion	General Hospital	Class 1	880.6990	2009-08-18
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2008-11-24
MWS	Stabilizer, Heart	Cardiovascular	Class 1	870.4500	2019-09-10

Official Correspondent

No official correspondent registered.

US Agent Details

Emily Valerio Email: emily.valerio@getinge.com Phone: (862) 2215193

Related Public Records

Same Entity

MAQUET (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
K812396	Northwest Surgical Concepts, Inc.	ARTHRO-PREP REST	1981-11-20

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007417753. Last updated year: 2026. Please use registration number 3007417753 when referencing this establishment in official correspondence.