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Access® Therapy

FDA UDI

Class Unclassified (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Access® Therapy FDA UDI
Generic Name
Multiple active implantable device programmer FDA UDI
Device Name
PROG 7436 KINETRA EZ PATNT ROHs US MKT FDA UDI
Model / Reference
7436 FDA UDI
Description
PROG 7436 KINETRA EZ PATNT ROHs US MKT FDA UDI

Identifiers

Primary DI / UDI-DI
00613994397836 FDA UDI
PMA Number
H050003 FDA UDI
P960009 FDA UDI
FDA Product Code
MFR FDA UDI
MHY FDA UDI
NHL FDA UDI
OLM FDA UDI
PJS FDA UDI
GMDN Term
Multiple active implantable device programmer FDA UDI

Classification

Device Class
Unclassified 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

No

FDA UDI

Category: Multiple active implantable device programmer

Access® Therapy by Medtronic, Inc. — Class Unclassified — 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

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI edbc68d1-7f74-4937-a256-d03eff8b411f 36 fields · synced May 30, 2026