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Accu-Beam

FDA UDI

Class I (US FDA UDI)

by Transamerican Technologies International

Identity

Trade Name
Accu-Beam FDA UDI
Generic Name
Surgical video camera FDA UDI
Device Name
Single chip video camera without recorder. 1080p 60hz, HDMI output. FDA UDI
Model / Reference
TTI-HD FDA UDI
Description
Single chip video camera without recorder. 1080p 60hz, HDMI output. FDA UDI

Identifiers

Primary DI / UDI-DI
B177TTIHD0 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Surgical 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical video camera

Accu-Beam by Transamerican Technologies International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 69820fea-1e2c-4804-89bb-493edb89d833 33 fields · synced Jun 9, 2026