Is this your brand? Sign in to claim ownership.

B BRAUN INTERVENTIONAL SYSTEMS, INC

Last updated May 24, 2026

What B BRAUN INTERVENTIONAL SYSTEMS, INC makes

The company manufactures interventional cardiovascular and vascular devices, including cardiac valvuloplasty catheters for treating narrowed heart valves, bare-metal and stent-graft systems for aortic interventions, and peripheral angioplasty balloons for treating blocked arteries. Additional products include vascular catheter introduction sets, vascular ports and catheters for long-term access, and multi-purpose drainage catheters for abdominal or thoracic fluid management. Cardiac sizing catheters are also part of the portfolio, used to measure valve annulus dimensions before procedures.

The device portfolio spans FDA device classes, with Class I products for minimally invasive accessories, Class II for moderate-risk items like angioplasty balloons and vascular ports, and Class III for high-risk interventions such as aortic stents and valvuloplasty catheters. All listed devices are registered in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The company is headquartered in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: bbraun.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(877)836-2228
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 784259751

Catalogue (1693)

Page 19 of 34

Device	Model / Reference	Registries	Class	Status
Mini Ghost™	612758	FDA UDI	Class II	Unknown
Mini Ghost™	613809	FDA UDI	Class II	Active
CP Stent™	614474	FDA UDI	Class III	Active
Pts®	613707	FDA UDI	Class II	Active
Z-Med™	610477	FDA UDI	Class II	Active
CP Stent™	614311	FDA UDI	Class III	Active
Z-Med X™	618431	FDA UDI	Class II	Active
CP Stent™	614375	FDA UDI	Class III	Active
Accel®	613915	FDA UDI	Class I	Active
Tyshak X™	618320	FDA UDI	Class II	Active
Pts-X™	613743	FDA UDI	Class II	Active
TYSHAK NuCLEUS™	612063	FDA UDI	Class II	Unknown
Z-Med Ii X™	618744	FDA UDI	Class II	Active
Accel®	612138	FDA UDI	Class II	Active
TYSHAK NuCLEUS™	612074	FDA UDI	Class II	Unknown
Mini Ghost™	612512	FDA UDI	Class II	Active
Mini Ghost™	612557	FDA UDI	Class II	Active
NuDEL	614571	FDA UDI	Class III	Active
Z-Med Ii X™	618709	FDA UDI	Class II	Unknown
Mini Ghost™	612539	FDA UDI	Class II	Active
Accel®	613907	FDA UDI	Class I	Active
Mini Ghost™	612681	FDA UDI	Class II	Unknown
Tyshak Ii®	611531	FDA UDI	Class II	Active
Celsite	5433742	FDA UDI	Class II	Active
B.braun	613406	FDA UDI	Class II	Unknown
Mini Ghost™	612690	FDA UDI	Class II	Unknown
CP Stent™	614319	FDA UDI	Class III	Active
Celsite	5430146	FDA UDI	Class II	Unknown
G-Armor Stent®	614746	FDA UDI	Class III	Active
Z-Med Ii™	611728	FDA UDI	Class II	Unknown
Z-Med™	610464	FDA UDI	Class II	Unknown
COEfficient™	611691	FDA UDI	Class III	Active
Z-Med Ii X™	618704	FDA UDI	Class II	Unknown
NuCLEUS-X™	612021	FDA UDI	Class II	Active
Z-Med Ii X™	618711	FDA UDI	Class II	Active
CP Stent™	614304	FDA UDI	Class III	Active
CP Stent™	614528	FDA UDI	Class III	Active
Bib®	614403	FDA UDI	Class II	Active
Z-Med™	611787	FDA UDI	Class II	Active
Mini Ghost™	612546	FDA UDI	Class II	Active
Tyshak X™	618331	FDA UDI	Class II	Active
Z-Med Ii X™	618752	FDA UDI	Class II	Active
Micro-Access Elite®	613349	FDA UDI	Class II	Unknown
Z-Med Ii X™	618717	FDA UDI	Class II	Active
Mini Ghost™	612684	FDA UDI	Class II	Active
COEfficient™	611205	FDA UDI	Class III	Active
Accel®	613921	FDA UDI	Class II	Active
Tyshak®	610518	FDA UDI	Class II	Unknown
Z-Med™	610469	FDA UDI	Class II	Active
Tyshak®	610544	FDA UDI	Class II	Unknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (4)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

B. Braun Interventional Systems, Inc. has four recall records initiated between October 30, 2007, and June 16, 2015, all of which are marked as terminated. The recalls involved incorrect components in needle accessories for Celsite Access Ports, reports of polyurethane catheter disconnections, out-of-specification endotoxin test results for peelable sheaths, and compromised package sealing on Tyvek pouches, leaving one edge partially open.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jun 16, 2015	Z-2382-2015	—	terminated	The manufacturer, B. Braun medical France, received endotoxin test results that are out of specification for the peelable sheath (A1537).
Apr 13, 2011	Z-2671-2011	—	terminated	The affected products contain the incorrect winged Surecan needle accessory component in certain Celsite Access Port package configurations. The winged Surecan needle is used to deliver medications and fluids into implanted Celsite Access Ports. Two winged Surecan needle sizes are provided in Celsite U.S. package configurations: 20G (PN 4058631) or 22G (PN 16006593A). A 20G or 22G needle
Jun 22, 2009	Z-1961-2009	—	terminated	B. Braun Interventional Systems was notified by B. Braun Medical France, the manufacturer of the Celsite Access port that they had received 11 reports of polyurethane (type P) catheter disconnections. B. Braun Medical France has decided to recall all Celsite ports supplied with the affected catheter lot. To date, B. Braun Interventional Systems (US) has not received any reports of catheter dis
Oct 30, 2007	Z-0264-2008	—	terminated	Sterility (package integrity) compromised: package sealing problem leaving packaging being partially open on one of the four sealed Tyvek pouch edges.