Cephalostat

FDA UDI

Class II (US FDA UDI)

by Carestream Dental LLC

Identity

Trade Name: CEPHALOSTAT FDA UDI
Generic Name: Stationary cephalometric x-ray system, digital FDA UDI
Device Name: CEPH UPGRADE FOR 9X00 FAMILY FDA UDI
Model / Reference: CEPHALOSTAT FDA UDI
Description: CEPH UPGRADE FOR 9X00 FAMILY FDA UDI

Identifiers

Catalog Number: 5211016 FDA UDI
Primary DI / UDI-DI: 60192155211010 FDA UDI
FDA Product Code: MUH FDA UDI
OAS FDA UDI
GMDN Term: Stationary cephalometric x-ray system, digital FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.1800 FDA UDI
892.1750 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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Stationary cephalometric x-ray system, digital

Cephalostat by Carestream Dental LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

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CS 8100SC 3D — CARESTREAM HEALTH, INC. · Class II
CS 9300C Select — CARESTREAM HEALTH, INC. · Class II
CS 8100SC — CARESTREAM HEALTH, INC. · Class II
Midmark Vantage Cephalometric Sensor — Midmark Corporation · Class II
Ceph attachment with sensor — Midmark Corporation · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Carestream Dental LLC

Sources (1)

FDA UDI 05cc884f-bd00-4b2b-a69c-506180736035 34 fields · synced Jun 8, 2026