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Activa® PC

FDA UDI

Class Unclassified (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Activa® PC FDA UDI
Generic Name
Deep brain electrical stimulation system FDA UDI
Device Name
INS 37601 ACTIVA PC DBS EMANUAL EN FDA UDI
Model / Reference
37601 FDA UDI
Description
INS 37601 ACTIVA PC DBS EMANUAL EN FDA UDI

Identifiers

Primary DI / UDI-DI
00763000310332 FDA UDI
PMA Number
H020007 FDA UDI
H050003 FDA UDI
P960009 FDA UDI
FDA Product Code
OLM FDA UDI
MRU FDA UDI
MHY FDA UDI
NHL FDA UDI
MBX FDA UDI
PJS FDA UDI
GMDN Term
Deep brain electrical stimulation system FDA UDI

Classification

Device Class
Unclassified 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Deep brain electrical stimulation system

Activa® PC by Medtronic, Inc. — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Deep brain electrical stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 1a83b0c4-41f0-46f6-8376-c70cc342844c 36 fields · synced May 31, 2026