JOAN LAB EQUIPMENT (ZHEJIANG) CO.,LTD.

FDA Device Registration & Listing · Huzhou Zhejiang, CN · Registration 3033848228

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
3033848228
FEI Number
3033848228
Entity Name
JOAN LAB EQUIPMENT (ZHEJIANG) CO.,LTD.
City/State/Country
Huzhou Zhejiang, CN
Establishment Address
ROOM 105, FLOOR 1, BUILDING 1, NO. 181, GANGFENG ROAD, KANGSHAN STREET, Huzhou Zhejiang 313000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
JOAN LAB EQUIPMENT (ZHEJIANG) CO.,LTD. (Owner Number: 10091674)
Owner / Operator Contact Address
ROOM 105, FLOOR 1, BUILDING 1, NO. 181, GANGFENG ROAD, KANGSHAN STREET, Huzhou, CN-ZJ 313000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DB100-2P MDB-100C,MDB-100,DB-100C,DB-100,MD100-2P,DB-100G,DB-100CG,DBSC-100Max,DBS-100Max DRY BATH MC-16Pro,LC-8P, LC5000H, HC500,HC500C,LC500C,LC800,LC800C,DM1424,DM1224, LAB CENTRIFUGE: LC-6S,LC-8S,LC-12S LAB CENTRIFUGE: LC300,LC500-8,LC500-12,LC500-6,LC500-18,LC500-24,LC500-8P,LC500-12P,LC500-MP LAB CENTRIFUGE: MC-4,MC-4K,MC-7K,MC-10K,MC-12K,MC-7S,MC-4/7S,MC-5Pro,MC-7Pro,MC-10Pro,MC-12Pro,MC-13Pro,MC-15Pro JN-8000R,NextSpin,JN-1850 LC-400,LC-400pro,LC-400P,JN-17000R

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JRG Block, Heating Clinical Chemistry Class 1 862.2050 2025-01-15
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2024-10-23

Official Correspondent

Summer Xia

US Agent Details

Peter Yang Business: JIAMEI CONSULTING INC. Email: info@jiameiconsulting.com Phone: (310) 2168437

Related Public Records

Same Entity

JOAN LAB EQUIPMENT (ZHEJIANG) CO.,LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033848228. Last updated year: 2026. Please use registration number 3033848228 when referencing this establishment in official correspondence.
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