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Lantern Delivery Catheter

FDA UDI

Class II (US FDA UDI)

by Penumbra, Inc.

Identity

Trade Name
Lantern Delivery Catheter FDA UDI
Generic Name
Vascular microcatheter FDA UDI
Device Name
PXSLIMLAN115T45 FDA UDI
Model / Reference
PXSLIMLAN115T45 FDA UDI
Description
PXSLIMLAN115T45 FDA UDI

Identifiers

Primary DI / UDI-DI
00814548016627 FDA UDI
510(k) Number
K152840 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Vascular microcatheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular microcatheter

Lantern Delivery Catheter by Penumbra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular microcatheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Penumbra, Inc.

Sources (1)

  • FDA UDI 9d5b869d-e376-4c74-af62-c4e5815f888c 34 fields · synced May 29, 2026