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FocESS

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
FocESS FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
HD Wireless Camera FDA UDI
Model / Reference
WCS FDA UDI
Description
HD Wireless Camera FDA UDI

Identifiers

Catalog Number
WCS-100 FDA UDI
Primary DI / UDI-DI
00857326005567 FDA UDI
FDA Product Code
FWL FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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

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: Endoscope video camera

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

Similar devices

Also classified as Endoscope video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI d826fd3c-9c2b-4888-b4d2-c1a21e5df2c4 34 fields · synced Jun 8, 2026