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Neptune

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Neptune FDA UDI
Generic Name
Suction system filter, plume particulate FDA UDI
Device Name
Smoke Tubing, Canister, Fluid Trap FDA UDI
Model / Reference
0703-045-100 FDA UDI
Description
Smoke Tubing, Canister, Fluid Trap FDA UDI

Identifiers

Catalog Number
0703-045-100 FDA UDI
Primary DI / UDI-DI
07613327471519 FDA UDI
FDA Product Code
QGI FDA UDI
GMDN Term
Suction system filter, plume particulate FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5080 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suction system filter, plume particulate

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

Similar devices

Also classified as Suction system filter, plume particulate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 6b41050f-a680-49ff-b8d4-07c2370cc6df 36 fields · synced May 30, 2026