← Back to catalogue

Advisor™ HD Grid X, Sensor Enabled™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Advisor™ HD Grid X, Sensor Enabled™ FDA UDI
Generic Name
Cardiac mapping catheter, percutaneous, single-use FDA UDI
Device Name
High Density Mapping Catheter FDA UDI
Model / Reference
D-AVHDX-DF16 FDA UDI
Description
High Density Mapping Catheter FDA UDI

Identifiers

Catalog Number
D-AVHDX-DF16 FDA UDI
Primary DI / UDI-DI
05415067049889 FDA UDI
510(k) Number
K241372 FDA UDI
FDA Product Code
MTD FDA UDI
GMDN Term
Cardiac mapping catheter, percutaneous, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1220 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 110.0000 Centimeter FDA UDI
Catheter Gauge — 8.0000 French FDA UDI

Category: Cardiac mapping catheter, percutaneous, single-use

Advisor™ HD Grid X, Sensor Enabled™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac mapping catheter, percutaneous, single-use.

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
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI 72b0c5d9-107a-492f-8785-37d3ca5635a2 38 fields · synced Jun 8, 2026