PULNOVO MEDICAL (WUXI) CO., LTD.

FDA Device Registration & Listing · Wuxi Jiangsu, CN · Registration 3041086754

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
3041086754
FEI Number
3041086754
Entity Name
PULNOVO MEDICAL (WUXI) CO., LTD.
City/State/Country
Wuxi Jiangsu, CN
Establishment Address
3rd Floor, Building D17, No.1719-17 Huishan Avenue and 3rd Floor, Building D11, No.1719-11 Huishan Avenue Huis, Wuxi Jiangsu 214000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Pulnovo Medical (Wuxi) Co., Ltd. (Owner Number: 10095366)
Owner / Operator Contact Address
3rd Floor, Building D17, No.1719-17 Huishan Avenue and 3rd Floor, Building D11, No.1719-11 Huishan Avenue Huis, Wuxi, CN-JS 214000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

PFlexi

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DYB Introducer, Catheter Cardiovascular Class 2 870.1340 2026-03-04

Official Correspondent

Cynthia Chen

US Agent Details

Semih Oktay Business: CardioMed Device Consultants LLC Email: soktay@cardiomedllc.com Phone: (410) 2712088

Related Public Records

Same Entity

Pulnovo Medical (Wuxi) 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
K101883 St Jude Medical 6F ENGAGE/ENGAGE TR INTRODUCER 2010-09-07
K034025 Nmt Medical, Inc. NMT MEDICAL TRANSSEPTAL SHEATH SET, MODELS TSS-10-HSC, TSS-11-HSC, TSS12-HSC 2004-03-26
K122854 Arrow International (Subsidiary of Teleflex Inc.) ARROW GLIDETHRU PEEL-AWAY SHEATH/DILATOR INTRODUCER 2013-01-04
K233691 Acutus Medical, Inc. FlexCath Cross Transseptal Solution 2023-12-17
K915078 North American Instrument Corp. MORSE HEMOSTATIC CATHETER INTRODUCER SET 1992-06-10

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0783-2020 Abbott Medical 2
Fast-Cath Trio HEMOSTASIS INTRODUCER, 14F, 4.6 mm, REF 406303
Z-0789-2020 Abbott Medical 2
Fast-Cath Hemostasis Introducer, HEMOSTASIS INTRODUCER, 8.5F, 2.83 mm, REF 406143 - Product Usage: The Fast-Cath Hemostasis Introducers are indicated for the introduction of angiographic catheters, closed-end catheters, balloon catheters, and electrodes into a vessel where minimizing blood loss is essential.

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3013300026 BIOSENSE WEBSTER, INC. Irvine, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3041086754. Last updated year: 2026. Please use registration number 3041086754 when referencing this establishment in official correspondence.
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