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Trinity

FDA UDI

Class II (US FDA UDI)

by Santa Barbara Imaging Systems, Inc.

Identity

Trade Name
Trinity FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
TRINITY 4K Camera Head 3 CMOS - C-MOUNT FDA UDI
Model / Reference
81-10-4130 FDA UDI
Description
TRINITY 4K Camera Head 3 CMOS - C-MOUNT FDA UDI

Identifiers

Catalog Number
81-10-4130 FDA UDI
Primary DI / UDI-DI
00853460007313 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscope video camera 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope video camera

Trinity by Santa Barbara Imaging Systems, Inc. — Class II — 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
Santa Barbara Imaging Systems, Inc.

Sources (1)

  • FDA UDI c0e6b3f5-bf05-4a50-8407-0b1227cc517e 35 fields · synced May 30, 2026