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Prowler

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
PROWLER FDA UDI
Generic Name
Vascular microcatheter FDA UDI
Device Name
PROWLER SELECT LP ES microcatheter FDA UDI
Model / Reference
MC1755S2U FDA UDI
Description
PROWLER SELECT LP ES microcatheter FDA UDI

Identifiers

Catalog Number
MC1755S2U FDA UDI
Primary DI / UDI-DI
10886704085584 FDA UDI
510(k) Number
K214025 FDA UDI
FDA Product Code
DQY FDA UDI
QJP FDA UDI
KRA FDA UDI
GMDN Term
Vascular microcatheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
870.1210 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular microcatheter

Prowler by Medos International Sàrl — 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

Sources (1)

  • FDA UDI 6bc41d50-f816-4de3-b070-dd79fd2445b9 36 fields · synced May 30, 2026