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Sprinter Legend

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
SPRINTER LEGEND FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Device Name
BLN SPL12506WL SPR LEGEND 1.25X6 OTW US FDA UDI
Model / Reference
SPL12506WL FDA UDI
Description
BLN SPL12506WL SPR LEGEND 1.25X6 OTW US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169018983 FDA UDI
510(k) Number
K103095 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
Outer Diameter — 1.25 Millimeter FDA UDI
Length — 6.0 Millimeter FDA UDI

Category: Coronary angioplasty balloon catheter, basic

Sprinter Legend 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 cd94ef37-bca3-4bf6-af01-60aa5be06c11 36 fields · synced May 30, 2026