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Spy

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SPY FDA UDI
Generic Name
Rigid optical cystoscope FDA UDI
Model / Reference
0502720030 FDA UDI

Identifiers

Catalog Number
0502-720-030 FDA UDI
Primary DI / UDI-DI
07613327616736 FDA UDI
510(k) Number
K233635 FDA UDI
FDA Product Code
NWB FDA UDI
FAJ FDA UDI
HIH FDA UDI
GMDN Term
Rigid optical cystoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
884.1690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 30.0 Centimeter FDA UDI

Category: Rigid optical cystoscope

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

Similar devices

Also classified as Rigid optical cystoscope.

Cleared under the same submission

K233635 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI ef26e8e3-861f-4295-a89b-ee50bf7ef9ce 36 fields · synced May 30, 2026