Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9612452

FEI Number

3002806713

Entity Name

B. BRAUN MEDICAL

City/State/Country

CHASSENEUIL-DU-POITOU Vienne, FR

Establishment Address

30 AVENUE DES TEMPS MODERNES, CHASSENEUIL-DU-POITOU Vienne 86360, FR

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

B. BRAUN MEDICAL SAS (Owner Number: 8023036)

Owner / Operator Contact Address

26 Rue Armengaud, Saint-Cloud, FR-NOTA 92210, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K170897

PMA Number

N/A

All Registered Proprietary Names

VenaTech Convertible Vena Cava Filter System VenaTech LP Vena Cava Filter System Venatech LP Brachial Introducer System (Antecubital) Celsite Babyport Celsite Celsite Babyport S Surecan Safety II

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DTK	Filter, Intravascular, Cardiovascular	Cardiovascular	Class 2	870.3375	2024-09-04
DTK	Filter, Intravascular, Cardiovascular	Cardiovascular	Class 2	870.3375	2009-10-20
LJT	Port & Catheter, Implanted, Subcutaneous, Intravascular	General Hospital	Class 2	880.5965	2013-11-26
PTI	Non-Coring (Huber) Needle	General Hospital	Class 2	880.5570	2017-11-29

Official Correspondent

No official correspondent registered.

US Agent Details

Kamaal Anas Business: B. Braun Medical, Inc. Email: kamaal.anas@bbraunusa.com Phone: (484) 5231349

Related Public Records

Same Entity

B. BRAUN MEDICAL SAS

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
K912423	Med Institute, Inc.	VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112	1991-07-30
K961652	Arrow Intl., Inc.	LOW PROFILE PLASTIC PORT DETACHED CATHETER SYSTEM CATALOG #1017	1996-07-19
K893460	Therex Corp.	A-PORT IMPLANT VASCULAR ACCESS SYSTEM .6MM/2.29MM	1989-06-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9612452. Last updated year: 2026. Please use registration number 9612452 when referencing this establishment in official correspondence.