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Ceph attachment with sensor

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Ceph attachment with sensor FDA UDI
Generic Name
Stationary cephalometric x-ray system, digital FDA UDI
Device Name
Ceph attachment with sensor FDA UDI
Model / Reference
C6000 FDA UDI
Description
Ceph attachment with sensor FDA UDI

Identifiers

Catalog Number
C6000 FDA UDI
Primary DI / UDI-DI
00841709102752 FDA UDI
FDA Product Code
MUH 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
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

Yes

FDA UDI

Category: Stationary cephalometric x-ray system, digital

Ceph attachment with sensor by Midmark Corporation — 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

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 88aad3cc-ab25-42da-aa66-979cb8d2947a 36 fields · synced Jun 8, 2026