← Back to catalogue

Mariner

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
Mariner FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
Mariner Hydrophilic Coated Angiographic Catheter, MPA, Braided FDA UDI
Model / Reference
11735503 FDA UDI
Description
Mariner Hydrophilic Coated Angiographic Catheter, MPA, Braided FDA UDI

Identifiers

Primary DI / UDI-DI
H787117355030 FDA UDI
510(k) Number
K112452 FDA UDI
K161596 FDA UDI
K173762 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Angiographic catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

Dimensions & Sizes

Size
Length — 80 Centimeter FDA UDI
Catheter Gauge — 5 French FDA UDI

Category: Angiographic catheter, single-use

Mariner by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Cleared under the same submission

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
Angiodynamics, Inc

Sources (1)

  • FDA UDI a8775f77-b052-42dd-b8f1-4da678e2d918 37 fields · synced Jun 20, 2026