International Medical Devices Database

17 devices in the database

BARD MAXCORE Disposable Core Biopsy Instrument

Model / Serial
Lot Numbers: REBP0019, REBN0342, REBN2123, REBP1199, REBP1419, REBP1807, REBQ0084, REBQ0343, REBQ1012, REBP1420, REBP1809, REBP0869, REBP1266, REBP1267, REBP1421, REBP1422, REBP1810, REBQ0087, REBQ0088, REBQ0347, REBQ0811, REBQ1014, REBP0158, REBQ1904, REBQ1898, REBQ1978, REBR0468, REBQ2296, REBR0474
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
US, Australia, Canada, Europe, Middle East, Africa, Latin America, Asia Pacific
Product Description
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.

SEEKER(R) Crossing Support Catheter

Model / Serial
UDI: (01)00801741067907(17)191207(10)VTBZ0193, Lot Number: VTBZ0193
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.014", 150 cm, REF SK15014. || Intended to support a guidewire during access into the vasculature.

SEEKER(R) Crossing Support Catheter

Model / Serial
UDI: (01)00801741067921(17)191115(10)VTBY0563, Lot Number: VTBY0563
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.035", 150 cm, REF SK15035M. || Intended to support a guidewire during access into the vasculature.

Device Recall POWERPORT(R) ClearVUE(R) Slim Implantable Port with Smooth Septum and Attachable 8...

Model / Serial
Lot Number Unique Device Identifier (UDI) REAN0056 (01)00801741110894(17)170628(10)REAN0056 REAN0203 (01)00801741110894(17)170628(10)REAN0203 REAP0773 (01)00801741110894(17)170728(10)REAP0773 REBN0925 (01)00801741110894(17)180131(10)REBN0925
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide
Product Description
POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005

Device Recall POWERPORT(R) ClearVUE(R) isp Implantable Port With Smooth Septum and Attachable 8F...

Model / Serial
Lot Number Unique Device Identifier (UDI) REAN0057 (01)00801741110887(17)170628(10)REAN0057 REAN0204 (01)00801741110887(17)170628(10)REAN0204 REAP0770 (01)00801741110887(17)170728(10)REAP0770 REBP0837 (01)00801741110887(17)180131(10)REBP0837
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide
Product Description
POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00004

12 more

7 manufacturers with a similar name

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Bard Peripheral Vascular Inc

Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
NZMMDSA

Bard Peripheral Vascular Inc

Manufacturer Address
Bard Peripheral Vascular Inc, 1625 W 3rd St Ste 109, Tempe AZ 85281-2438
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
USFDA

Bard Peripheral Vascular Inc

Manufacturer Address
Bard Peripheral Vascular Inc, 1625 W 3rd St, Tempe AZ 85281-2438
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
USFDA

Bard Peripheral Vascular Inc.

Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
BAM

Bard Peripheral Vascular Inc. (BPV)

Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
BAM

2 more

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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