← Back to catalogue

Stryker

FDA UDI

Class I (US FDA UDI)

by Barco, Inc.

Identity

Trade Name
Stryker FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
3G-SDI to HDMI Converter FDA UDI
Model / Reference
0240-099-260 FDA UDI
Description
3G-SDI to HDMI Converter FDA UDI

Identifiers

Primary DI / UDI-DI
00700621719571 FDA UDI
FDA Product Code
FWB FDA UDI
GMDN Term
Endoscopic video image processing unit 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

Stryker by Barco, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Barco, Inc.

Sources (1)

  • FDA UDI 7de8ed2d-35cb-4967-8215-2a45cce8fa7c 34 fields · synced May 30, 2026