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Trinity 81-10-2130

by Santa Barbara Imaging Systems, Inc.

Trinity 81-10-2130 is a Class II device made by Santa Barbara Imaging Systems, Inc., listed in FDA GUDID since 8 Jan 2019 (UDI-DI 00853460007306), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00853460007306 UDI-DI Date8 Jan 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Trinity
Generic name
Endoscope video camera
Model / Ref / Catalog
81-10-2130
Primary DI / UDI-DI
00853460007306
FDA product code
GCJ
GMDN term
Endoscope video camera
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscope video camera

Other devices from Santa Barbara Imaging Systems, Inc.

See all devices from Santa Barbara Imaging Systems, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)