← Back to catalogue

BurstDR™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
BurstDR™ FDA UDI
Generic Name
Multiple active implantable device programmer FDA UDI
Device Name
Patient Programmer FDA UDI
Model / Reference
Stimulation Temp Evaluation FDA UDI
Description
Patient Programmer FDA UDI

Identifiers

Catalog Number
3857 FDA UDI
Primary DI / UDI-DI
05415067028709 FDA UDI
PMA Number
P010032 FDA UDI
FDA Product Code
LGW 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Multiple active implantable device programmer

BurstDR™ 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.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 7838e46d-820f-40a0-98f2-b20990a57ce6 37 fields · synced May 30, 2026