BECTON DICKINSON GMBH

FDA Device Registration & Listing · HEIDELBERG Baden-Wurttemberg, DE · Registration 9680577

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
9680577
FEI Number
1000366600
Entity Name
BECTON DICKINSON GMBH
City/State/Country
HEIDELBERG Baden-Wurttemberg, DE
Establishment Address
TULLASTRASSE 8-12, HEIDELBERG Baden-Wurttemberg 69126, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Becton Dickinson and Company (Owner Number: 9922032)
Owner / Operator Contact Address
One Becton Drive, Franklin Lakes, NJ 07417, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ENTEROTUBE II

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JSS Kit, Identification, Enterobacteriaceae Microbiology Class 1 866.2660 2001-02-08

Official Correspondent

No official correspondent registered.

US Agent Details

Jeffrey Zinza Business: BECTON DICKINSON AND COMPANY Email: jeffrey.zinza@bd.com Phone: (858) 2093953

Related Public Records

Same Entity

Becton Dickinson and Company
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003916417 BECTON DICKINSON IND. CIRURGICAS LTDA. CURITIBA Parana, BR
3036495171 BD Biosciences San Diego San Diego, CA, US
3015292643 BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES San Diego, CA, US
3010141591 BD Kiestra B.V. Drachten Fryslan, NL
9614033 BECTON DICKINSON DE MEXICO CUAUTITLAN, IZCALLI Queretaro, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K760790 General Diagnostics MICRO-ID 1976-10-29

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0022-2009 Becton Dickinson and Company 1
BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680577. Last updated year: 2026. Please use registration number 9680577 when referencing this establishment in official correspondence.
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