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Exodus

FDA UDI

Class II (US FDA UDI)

by Navilyst Medical, Inc.

Identity

Trade Name
Exodus FDA UDI
Generic Name
Nephrostomy catheter FDA UDI
Device Name
Nuance Nephrostomy Drainage Catheter 10F x 35cm with Tight Pigtail FDA UDI
Model / Reference
10518 FDA UDI
Description
Nuance Nephrostomy Drainage Catheter 10F x 35cm with Tight Pigtail FDA UDI

Identifiers

Primary DI / UDI-DI
H965105180 FDA UDI
510(k) Number
K152069 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Nephrostomy catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5010 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 — 25 Centimeter FDA UDI
Outer Diameter — 3.4 Millimeter FDA UDI
Catheter Gauge — 10 French FDA UDI

Category: Nephrostomy catheter

Exodus by Navilyst Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nephrostomy catheter.

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 2743d8ae-03a4-462b-b349-3e88c91bf76b 36 fields · synced Jun 6, 2026