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Rev360

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Rev360 FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI
Device Name
[Dimpled Vaporizing Roller Ball Electrode, 22 Fr., Only for use with Stryker Resectoscopes, Do not use if package is damaged] FDA UDI
Model / Reference
0504990600 FDA UDI
Description
[Dimpled Vaporizing Roller Ball Electrode, 22 Fr., Only for use with Stryker Resectoscopes, Do not use if package is damaged] FDA UDI

Identifiers

Catalog Number
0504-990-600 FDA UDI
Primary DI / UDI-DI
07613327055580 FDA UDI
FDA Product Code
FAJ FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Category: Endoscopic electrosurgical electrode, bipolar, single-use

Rev360 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, 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 787345c0-942e-499a-b070-4416f563d753 35 fields · synced May 30, 2026