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Cs 9300c

FDA UDI

Class II (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
CS 9300C FDA UDI
Generic Name
Stationary cephalometric x-ray system, digital FDA UDI
Device Name
CS 9300C 230V R FDA UDI
Model / Reference
CS 9300C FDA UDI
Description
CS 9300C 230V R FDA UDI

Identifiers

Catalog Number
5210968 FDA UDI
Primary DI / UDI-DI
60889975210964 FDA UDI
FDA Product Code
OAS FDA UDI
GMDN Term
Stationary cephalometric x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cone beam computed tomography system, head/neckStationary cephalometric x-ray system, digital

Cs 9300c by Carestream Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary cephalometric x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 77f2b82a-7c74-450d-b375-fb738febdd20 34 fields · synced Jun 8, 2026