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Nc Sprinter®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
NC SPRINTER® FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Device Name
BALLOON NCSP32521X NCSPRINTER RX M US FDA UDI
Model / Reference
NCSP32521X FDA UDI
Description
BALLOON NCSP32521X NCSPRINTER RX M US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169281974 FDA UDI
PMA Number
P790017 FDA UDI
FDA Product Code
LOX FDA UDI
GMDN Term
Coronary angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 21.0 Millimeter FDA UDI
Outer Diameter — 3.25 Millimeter FDA UDI

Category: Coronary angioplasty balloon catheter, basic

Nc Sprinter® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, basic.

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 fcb52abd-0f4f-4e38-a469-58dd801842a4 36 fields · synced May 30, 2026