← Back to catalogue

GORE TAG Conformable Thoracic Endoprosthesis

FDA UDI

Class III (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE TAG Conformable Thoracic Endoprosthesis FDA UDI
Generic Name
Descending thoracic aorta endovascular stent-graft FDA UDI
Device Name
TAG THORACIC ENDO CONFORM 28mmX10cm 20Fr FDA UDI
Model / Reference
TGU282810 FDA UDI
Description
TAG THORACIC ENDO CONFORM 28mmX10cm 20Fr FDA UDI

Identifiers

Catalog Number
TGU282810 FDA UDI
Primary DI / UDI-DI
00733132618026 FDA UDI
PMA Number
P040043 FDA UDI
FDA Product Code
MIH FDA UDI
GMDN Term
Descending thoracic aorta endovascular stent-graft FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 28 Millimeter FDA UDI
Length — 10 Centimeter FDA UDI

Category: Descending thoracic aorta endovascular stent-graft

GORE TAG Conformable Thoracic Endoprosthesis by W. L. Gore & Associates, Inc — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Descending thoracic aorta endovascular stent-graft.

Cleared under the same submission

P040043 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
W. L. Gore & Associates, Inc

Sources (1)

  • FDA UDI 251470ac-7b96-480b-9593-7904953961d2 37 fields · synced Jun 8, 2026