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Diacor Overlay

FDA UDIEUDAMED

Class II (US FDA UDI)

by Diacor Inc.

Identity

Trade Name
Diacor Overlay FDA UDI
Generic Name
Radiological whole-body positioner FDA UDI
Device Name
Radiation Oncology Flat Table Top (FTT) for GE Tandem D670 FDA UDI
Model / Reference
OGT-1 FDA UDI
Description
Radiation Oncology Flat Table Top (FTT) for GE Tandem D670 FDA UDI

Identifiers

Primary DI / UDI-DI
B237OGT10 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Radiological whole-body positioner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Radiological whole-body positioner

Diacor Overlay by Diacor Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Radiological whole-body positioner.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diacor Inc.

Sources (2)

  • FDA UDI 3b1b8077-e199-4518-b8d8-a5312320b176 34 fields · synced Jun 20, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026