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Selectsecure™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Selectsecure™ FDA UDI
Generic Name
Endocardial/interventricular septal pacing lead FDA UDI
Device Name
LEAD 383059 SELECTSECURE US DIR DISP FDA UDI
Model / Reference
383059 FDA UDI
Description
LEAD 383059 SELECTSECURE US DIR DISP FDA UDI

Identifiers

Primary DI / UDI-DI
00643169279292 FDA UDI
PMA Number
P030036 FDA UDI
FDA Product Code
NVY FDA UDI
DTB FDA UDI
NVN FDA UDI
GMDN Term
Endocardial/interventricular septal pacing lead FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.3680 FDA UDI
Commercial Distribution
Not 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

Yes

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

Dimensions & Sizes

Size
Length — 59.0 Centimeter FDA UDI

Selectsecure™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

P030036 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI ab1c2905-7434-4038-aa6b-7584f7ecc3e6 38 fields · synced May 31, 2026