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MediGuide™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
MediGuide™ FDA UDI
Generic Name
Cardiac mapping system FDA UDI
Device Name
MTAC FDA UDI
Model / Reference
Technology FDA UDI
Description
MTAC FDA UDI

Identifiers

Catalog Number
H700670 FDA UDI
Primary DI / UDI-DI
05415067006707 FDA UDI
510(k) Number
K120301 FDA UDI
FDA Product Code
DQK FDA UDI
GMDN Term
Cardiac mapping system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1425 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiac mapping system

MediGuide™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac mapping system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d82d1b84-3d84-4c6e-96e4-fa28b9fb80ff 37 fields · synced Jun 6, 2026