CareFusion D.R. 203 Ltd.

FDA Device Registration & Listing · SANTO DOMINGO Distrito Nacional, DO · Registration 9680904

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
9680904
FEI Number
3007019930
Entity Name
CareFusion D.R. 203 Ltd.
City/State/Country
SANTO DOMINGO Distrito Nacional, DO
Establishment Address
ZONA FRANCA LAS AMERICAS, KM 22 E-1, SANTO DOMINGO Distrito Nacional --, DO
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CAREFUSION (Owner Number: 10030506)
Owner / Operator Contact Address
75 N Fairway Dr, Vernon Hills, IL 60061, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Marquee™ Disposable Core Biopsy Instrument Marquee™ Disposable Core Biopsy Instrument Kit PeritX™ 2L Drainage Starter Pack PeritX™ 2L Drainage Starter Tote PeritX™ Peritoneal Catheter System PeritX™ 2L Drainage Kit Safe-T PLUS Tray Illinois Bone Marrow Aspiration Tray Illinois Bone Marrow Aspiration Needle T-Handle Illinois Bone Marrow Aspiration Needle T-Handle Illinois Bone Marrow Aspiration Tray Bard Mission Disposable Core Biopsy Instrument Kit Bard Mission Disposable Core Biopsy Instrument Bard Marquee Disposable Core Biopsy Instrument and Kit Chiba FNA Magnum™ Disposable Core Biopsy Needles

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2025-07-29
PNG Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling Gastroenterology, Urology Class 2 876.5630 2025-01-09
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2009-10-12
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2019-05-24
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2019-05-24
DWM Apparatus, Suction, Patient Care Cardiovascular Class 2 870.5050 2016-11-22
GAA Needle, Aspiration And Injection, Disposable General, Plastic Surgery Class 1 878.4800 2009-10-12
FCG Biopsy Needle Gastroenterology, Urology Class 2 876.1075 2021-07-29
GDF Guide, Needle, Surgical General, Plastic Surgery Class 1 878.4800 2009-10-12
FCG Biopsy Needle Gastroenterology, Urology Class 2 876.1075 2009-10-12
FSH Tray, Surgical, Needle General, Plastic Surgery Class 1 878.4800 2009-10-12

Official Correspondent

No official correspondent registered.

US Agent Details

Kristen Ortiz Email: kristen.ortiz@bd.com Phone: (602) 8305652

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
1625685 CAREFUSION 2200, INC. Mannford, OK, US
1423507 CAREFUSION 2200, INC. Vernon Hills, IL, US
3004932373 CareFusion 213 LLC EL PASO, TX, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09
K160450 Care Fusion Pleurx Pleural Catheter System 2016-10-31
K781371 Ferris Mfg. Corp. BONE MARROW ASPIRATION KIT 1978-09-20
K150891 Covidien, LLC( Formerly Beacon Endoscopic Corp.) BNX Fine Needle Aspiration System and SharkCore LG Fine Needle Biopsy System 2015-05-01

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680904. Last updated year: 2026. Please use registration number 9680904 when referencing this establishment in official correspondence.
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