Zhejiang Sorfa Life Science Research Co., Ltd.

FDA Device Registration & Listing · Hangzhou Zhejiang, CN · Registration 3006795767

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
3006795767
FEI Number
3006795767
Entity Name
Zhejiang Sorfa Life Science Research Co., Ltd.
City/State/Country
Hangzhou Zhejiang, CN
Establishment Address
No. 148 Longshan Road, Zhongguan Town, Deqing County, Hangzhou Zhejiang 313220, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Zhejiang Sorfa Life Science Research Co., Ltd. (Owner Number: 10023001)
Owner / Operator Contact Address
No. 148 Longshan Road, Zhongguan Town, Deqing County, Hangzhou, CN-ZJ 313220, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Disposable Sample Collection Kit ESR pipette Serological pipette Plastic Pipet Serological Pipette TRANSFER PIPETTE Media Bottle Plastic Bottle Disposable Sample Collction Kit, Disposable Sampling Tube; Sample Collector; Sample Storage Tube; Swab Transport Medium Centrifuge Tube Cell Culture Flask Cell Culture Plate Cell Culture Dish PCR Tube Cell Scraper Petri Dish Disposable Pipette Micro Tips Blender Bag, Sampling Bag Vacuum Filter System Erlenmeyer Shake Flask

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNK Container, Specimen Mailer And Storage, Non-Sterile Pathology Class 1 864.3250 2020-05-01
JRC Micro Pipette Clinical Chemistry Class 1 862.2050 2007-10-29
KJA Flask, Tissue Culture Hematology Class 1 864.2240 2022-06-02
MPQ Container, Specimen, Urine, Drugs Of Abuse, Over The Counter Pathology Class 1 864.3260 2022-06-02
KDT Container, Specimen Mailer And Storage, Sterile Pathology Class 1 864.3250 2020-05-16
KIZ Dish, Tissue Culture Hematology Class 1 864.2240 2022-06-02
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2022-06-02

Official Correspondent

zhengrong jiang

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Zhejiang Sorfa Life Science Research 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-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006795767. Last updated year: 2026. Please use registration number 3006795767 when referencing this establishment in official correspondence.
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