Identity
- Trade Name
- Relay Plus Thoracic Stent-Graft System FDA UDI
- Generic Name
- Descending thoracic aorta endovascular stent-graft FDA UDI
- Device Name
- Endovascular stent-graft system FDA UDI
- Model / Reference
- 28-M326250262390U FDA UDI
- Description
- Endovascular stent-graft system FDA UDI
Identifiers
- Catalog Number
- 28-M326250262390U FDA UDI
- Primary DI / UDI-DI
- 00843576102057 FDA UDI
- PMA Number
- P110038 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 26 Millimeter FDA UDILength — 250 Millimeter FDA UDICatheter Gauge — 23 French FDA UDI
Category: Descending thoracic aorta endovascular stent-graft
Relay Plus Thoracic Stent-Graft System by Bolton Medical Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Descending thoracic aorta endovascular stent-graft.
- CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC · Class III
- VALIANT® Captivia — MEDTRONIC, INC. · Class III
- GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis — W. L. GORE & ASSOCIATES, INC · Class III
- VALIANT® Captivia — MEDTRONIC, INC. · Class III
- CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC · Class III
- VALIANT® Captivia — MEDTRONIC, INC. · Class III
- GORE TAG Conformable Thoracic Endoprosthesis — W. L. GORE & ASSOCIATES, INC · Class III
- VALIANT® Captivia — MEDTRONIC, INC. · Class III
Cleared under the same submission
P110038 also covers:
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
- Relay Plus Thoracic Stent-Graft System — Bolton Medical Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bolton Medical Inc.
Sources (1)
- FDA UDI 8dc3feff-6851-4fda-8e4c-4e12b3f56002 37 fields · synced May 30, 2026