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Ares™

FDA UDI

Class II (US FDA UDI)

by Medtronic PS Medical

Identity

Trade Name
ARES™ FDA UDI
Generic Name
Lumboperitoneal shunt peritoneal catheter FDA UDI
Device Name
CATHETER 93092 DISTAL ANTIMICROBIAL FDA UDI
Model / Reference
93092 FDA UDI
Description
CATHETER 93092 DISTAL ANTIMICROBIAL FDA UDI

Identifiers

Primary DI / UDI-DI
00643169474949 FDA UDI
510(k) Number
K110560 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Lumboperitoneal shunt peritoneal catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 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

Yes

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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 120.0 Centimeter FDA UDI

Category: Lumboperitoneal shunt peritoneal catheter

Ares™ by Medtronic PS Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumboperitoneal shunt peritoneal catheter.

Cleared under the same submission

K110560 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic PS Medical

Sources (1)

  • FDA UDI 593a73d1-b160-4618-a008-5361994ea965 37 fields · synced May 30, 2026