Skip to content

Accu-Beam TTI-HD

by Transamerican Technologies International

Accu-Beam TTI-HD is a Class I device made by Transamerican Technologies International, listed in FDA GUDID since 23 Jul 2018 (UDI-DI B177TTIHD0), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB177TTIHD0 UDI-DI Date23 Jul 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Accu-Beam
Generic name
Surgical video camera
Model / reference
TTI-HD
Description
Single chip video camera without recorder. 1080p 60hz, HDMI output.
Primary DI / UDI-DI
B177TTIHD0
FDA product code
KQM
GMDN term
Surgical video camera
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical video camera

Similar devices in this category

Other devices filed under Surgical video camera.

Other devices from Transamerican Technologies International

See all devices from Transamerican Technologies International →

Properties

  • Premarket exempt
Other properties (14, all answered No)