Accu-Beam

FDA UDI

Class I (US FDA UDI)

by Transamerican Technologies International

Identity

Trade Name: Accu-Beam FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: Sterilization tray with silicone mat FDA UDI
Model / Reference: 1056521SM FDA UDI
Description: Sterilization tray with silicone mat FDA UDI

Identifiers

Primary DI / UDI-DI: B1771056521SM0 FDA UDI
FDA Product Code: FSM FDA UDI
GMDN Term: Instrument tray, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Transamerican Technologies International

Sources (1)

FDA UDI 6532c4e7-b2c3-4ea0-8284-1e510c74ab7b 33 fields · synced Jun 9, 2026