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Compu-Cutter 111

FDA UDI

Class II (US FDA UDI)

by Huestis Machine Corp.

Identity

Trade Name
Compu-Cutter 111 FDA UDI
Generic Name
Radiation therapy beam block production hot-wire FDA UDI
Device Name
Compu-cutter shielding bolck cutters cut foam block molds so that extremely precise alloy blocks can be made to shield patients during radiation treatment. FDA UDI
Model / Reference
CC3-1000 FDA UDI
Description
Compu-cutter shielding bolck cutters cut foam block molds so that extremely precise alloy blocks can be made to shield patients during radiation treatment. FDA UDI

Identifiers

Primary DI / UDI-DI
00850077007163 FDA UDI
510(k) Number
K940145 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiation therapy beam block production hot-wire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiation therapy beam block production hot-wire

Compu-Cutter 111 by Huestis Machine Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy beam block production hot-wire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Huestis Machine Corp.

Sources (1)

  • FDA UDI 0c00eb91-ee3f-4c34-bcb6-17fe01646055 34 fields · synced May 30, 2026