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SKATER™ All Purpose and Nephrostomy Drainage Set

FDA UDI

Class I (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
SKATER™ All Purpose and Nephrostomy Drainage Set FDA UDI
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Device Name
SKATER™ All Purpose and Nephrostomy Drainage Set Locking 14F x 35cm FDA UDI
Model / Reference
756614035 FDA UDI
Description
SKATER™ All Purpose and Nephrostomy Drainage Set Locking 14F x 35cm FDA UDI

Identifiers

Catalog Number
756614035 FDA UDI
Primary DI / UDI-DI
00886333225262 FDA UDI
FDA Product Code
GBO FDA UDI
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-purpose percutaneous abdominothoracic drainage catheter

SKATER™ All Purpose and Nephrostomy Drainage Set by Argon Medical Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose percutaneous abdominothoracic drainage catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Argon Medical Devices, Inc.

Sources (1)

  • FDA UDI 3d6a058e-b1e7-434c-9288-cec140ac6558 37 fields · synced Jun 9, 2026