Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

ANGIOSYSTEMS, INCORPORATED

US

Last updated May 23, 2026

What ANGIOSYSTEMS, INCORPORATED makes

Angiosystems, Incorporated manufactures medicated surgical procedure kits, single-use and reusable sterile drapes for surgical and angiographic procedures, and radiation shielding materials designed to protect patients from ionizing radiation. Their portfolio includes specialized trays for surgical applications, radiation-shielding pads and drapes, and camera covers for medical imaging equipment.

The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

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

Frequently asked questions

What types of medical devices does Angiosystems, Incorporated primarily manufacture?

Angiosystems, Incorporated specializes in surgical and radiation protection devices. Their portfolio includes medicated surgical procedure kits, single-use and reusable sterile drapes for general surgery and angiographic procedures, as well as radiation shielding materials like pads, drapes, and camera covers. These products are designed to enhance procedural safety and reduce patient exposure to ionizing radiation during medical imaging.

Where is Angiosystems, Incorporated based?

Angiosystems, Incorporated is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards, which govern the design, manufacturing, and distribution of its medical devices.

Which regulatory registries or databases list Angiosystems, Incorporated’s devices?

Angiosystems, Incorporated’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify product details, compliance, and device history.

How are Angiosystems, Incorporated’s devices classified under FDA regulations?

Angiosystems, Incorporated’s devices fall under three FDA classification categories: Class I (generally low-risk devices requiring minimal regulation), Class II (devices with moderate risk requiring special controls), and Unclassified (U) devices (those not yet assigned a risk category). Classification determines the regulatory pathway and oversight required for each product.

What is the purpose of the radiation shielding materials produced by Angiosystems, Incorporated?

The radiation shielding materials, such as the Halyard Scatter Radiation Shields and patient shielding pads/drapes, are designed to protect patients from ionizing radiation during procedures like fluoroscopy or angiography. These materials absorb or deflect radiation, reducing exposure risks while maintaining procedural visibility for medical staff.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
144884467

Catalogue (336)

Page 2 of 7
DeviceModel / ReferenceRegistriesClassStatus
AngioSystems Tray 5690
FDA UDI
Class IActive
AngioSystems Tray 5700
FDA UDI
Class IActive
AngioSystems Tray 5680-7
FDA UDI
Class IActive
AngioSystems SorbX SX5100
FDA UDI
Class IActive
AngioSystems SorbX SX8325
FDA UDI
Class IActive
AngioSystems Drape 3648-03
FDA UDI
Class IIActive
AngioSystems Tray KM5073
FDA UDI
Class IActive
AngioSystems Tray 5572
FDA UDI
Class IActive
AngioSystems Tray 5456
FDA UDI
Class IActive
Halyard Scatter Radiation Shields 48986 Multi-Purpose Shield W/ FEN L1
FDA UDI
Class IActive
AngioSystems Drape 3436
FDA UDI
Class IIActive
AngioSystems Tray 5680-4
FDA UDI
Class IActive
AngioSystems Tray 1056
FDA UDI
Class IActive
AngioSystems SorbX SX7110
FDA UDI
Class IActive
AngioSystems Drape 3215NS
FDA UDI
Class IIActive
AngioSystems SorbX SX7226
FDA UDI
Class IActive
AngioSystems Drape 5520
FDA UDI
Class IActive
AngioSystems Cap Cover 6004
FDA UDI
Class IActive
AngioSystems SorbX SX7257-1D
FDA UDI
Class IActive
Halyard Scatter Radiation Shields 48957 Multi Purpose Shield L1 NS
FDA UDI
Class IActive
AngioSystems Drape 3606-1
FDA UDI
Class IIActive
AngioSystems Tray KM5050-5
FDA UDI
Class IActive
AngioSystems SorbX SX7240
FDA UDI
Class IActive
AngioSystems Drape 3434NS
FDA UDI
Class IIActive
AngioSystems Drape 3663-01
FDA UDI
Class IIActive
AngioSystems Drape 3024-21
FDA UDI
Class IIActive
AngioSystems SorbX SX8232
FDA UDI
Class IActive
AngioSystems Tray KM5029
FDA UDI
Class IActive
AngioSystems Tray 3404599-1(3)
FDA UDI
Class IActive
AngioSystems Tray 43545-3
FDA UDI
Class IActive
AngioSystems Tray 5808
FDA UDI
Class IActive
AngioSystems Drape 3631
FDA UDI
Class IIActive
AngioSystems Tray 5021-1
FDA UDI
Class IActive
AngioSystems SorbX SX7101
FDA UDI
Class IActive
AngioSystems SorbX SX8231
FDA UDI
Class IActive
AngioSystems Tray KM5042
FDA UDI
Class IActive
AngioSystems Drape DR5-18063NS
FDA UDI
Class IIActive
AngioSystems Drape 3432-01
FDA UDI
Class IIActive
AngioSystems Drape 3003-13
FDA UDI
Class IIActive
AngioSystems Tray 5049
FDA UDI
Class IActive
AngioSystems Tray 5125
FDA UDI
Class IActive
AngioSystems Drape 3003-40
FDA UDI
Class IIActive
AngioSystems Tray KM5078
FDA UDI
Class IActive
AngioSystems Drape 3530
FDA UDI
Class IIActive
AngioSystems Tray KM5009
FDA UDI
Class IActive
AngioSystems SorbX SX8210
FDA UDI
Class IActive
Halyard Scatter Radiation Shields 49075 Jugular Shield Drape L2 NS
FDA UDI
Class IActive
AngioSystems Tray 5602-12
FDA UDI
Class IActive
AngioSystems Drape 6013
FDA UDI
Class IIActive
Halyard Scatter Radiation Shields 49069 Biopsy Shield Drape L2 NS
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.