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Neptune

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Neptune FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Device Name
SafeAir Smoke Evacuation Pencil, Push Button, Non-Coated, No PVC, Non-Sterile FDA UDI
Model / Reference
0703146003 FDA UDI
Description
SafeAir Smoke Evacuation Pencil, Push Button, Non-Coated, No PVC, Non-Sterile FDA UDI

Identifiers

Catalog Number
0703-146-003 FDA UDI
Primary DI / UDI-DI
07613327548273 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

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

Similar devices

Also classified as Open-surgery electrosurgical handpiece/electrode, monopolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI f31d15b8-b320-4a0e-8046-13cfc8b2746b 36 fields · synced May 29, 2026