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Neptune

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Neptune FDA UDI
Generic Name
Surgical fluid/smoke waste management system FDA UDI
Device Name
V2 4-PORT MANIFOLD FDA UDI
Model / Reference
0750400000 FDA UDI
Description
V2 4-PORT MANIFOLD FDA UDI

Identifiers

Catalog Number
0750400000 FDA UDI
Primary DI / UDI-DI
07613327563832 FDA UDI
FDA Product Code
JCX FDA UDI
GMDN Term
Surgical fluid/smoke waste management system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical fluid/smoke waste management system

Neptune by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical fluid/smoke waste management system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI e525069d-e41d-43c3-94f7-c91360fa86cf 35 fields · synced May 30, 2026