GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion PTB6104275

No FDA recalls found in the data synced 23 Oct 2026.

Trade Name

GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion

Generic Name

Endoprosthetic portosystemic shunt

Model / Ref / Catalog

PTB6104275

Primary DI / UDI-DI

00733132664177

PMA Number

P040027 ↗

FDA Product Code

MIR

GMDN Term

Endoprosthetic portosystemic shunt

Device Class

Class III

GUDID distribution status

In Commercial Distribution

MRI Safety

MR Conditional

• GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis

  Class III

  CE/MDR MDR 732278 Expiring Valid to Feb 2027

• GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface

  Class III

  CE/MDR MDR 731181 Active Valid to Jul 2031

• GORE-TEX® Stretch Vascular Graft

  Class III

  CE/MDR MDR 732281 Active Valid to Jul 2031

• GORE® EXCLUDER® Iliac Branch Endoprosthesis

  Class III

  CE/MDR MDR 731176 Active Valid to Jul 2031

• GORE® DrySeal Flex Introducer Sheath

  Class III

  CE/MDR MDR 764343 Active Valid to Apr 2028

• GORE® EXCLUDER® Conformable AAA Endoprosthesis

  Class III

  CE/MDR MDR 731175 Active Valid to Jul 2031

See all devices from W. L. Gore & Associates, Inc. →