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Wi-Fi™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Wi-Fi™ FDA UDI
Generic Name
Multiple active implantable device programmer FDA UDI
Device Name
Wi-Fi Card FDA UDI
Model / Reference
EX3213 FDA UDI
Description
Wi-Fi Card FDA UDI

Identifiers

Catalog Number
EX3213 FDA UDI
Primary DI / UDI-DI
05414734506830 FDA UDI
FDA Product Code
LWS FDA UDI
LWP FDA UDI
NKE FDA UDI
NIK FDA UDI
OSR FDA UDI
GMDN Term
Multiple active implantable device programmer FDA UDI

Classification

Device Class
Class III 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple active implantable device programmer

Wi-Fi™ by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple active implantable device programmer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI 3c6c5cd2-a383-473a-97fc-db49c48270ce 35 fields · synced Jun 8, 2026