← Back to catalogue

Pacific™ Plus

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Pacific™ Plus FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name
CATH PCP025040150 PCP D2.50 L 040 UL 150 FDA UDI
Model / Reference
PCP025040150 FDA UDI
Description
CATH PCP025040150 PCP D2.50 L 040 UL 150 FDA UDI

Identifiers

Primary DI / UDI-DI
08033477074856 FDA UDI
510(k) Number
K123358 FDA UDI
FDA Product Code
DQY FDA UDI
LIT FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
Commercial Distribution
Not 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 — 2.5 Millimeter FDA UDI
Length — 40.0 Millimeter FDA UDI

Pacific™ Plus by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K123358 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 35ba1c95-7aea-4dd5-8728-b03f32083829 38 fields · synced May 31, 2026