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Sun Nuclear CT Electron Density Phantom

FDA UDI

Class I (US FDA UDI)

by Sun Nuclear Corp.

Identity

Trade Name
Sun Nuclear CT Electron Density Phantom FDA UDI
Generic Name
CT phantom, test object FDA UDI
Model / Reference
467 FDA UDI

Identifiers

Primary DI / UDI-DI
B1364670 FDA UDI
FDA Product Code
LHO FDA UDI
GMDN Term
CT phantom, test object FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1940 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

Yes

FDA UDI

Category: CT phantom, test object

Sun Nuclear CT Electron Density Phantom by Sun Nuclear Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CT phantom, test object.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sun Nuclear Corp.

Sources (1)

  • FDA UDI b81c0b20-eb68-4f30-b15b-f95b79f6cb93 32 fields · synced Jun 6, 2026