Identity
- Trade Name
- Ceph Attachmetnt without sensor FDA UDI
- Generic Name
- Stationary cephalometric x-ray system, digital FDA UDI
- Device Name
- Ceph Attachment without sensor FDA UDI
- Model / Reference
- C4000 FDA UDI
- Description
- Ceph Attachment without sensor FDA UDI
Identifiers
- Catalog Number
- C4000 FDA UDI
- Primary DI / UDI-DI
- 00841709102745 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 Attachmetnt without sensor by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Midmark Corporation
Sources (1)
- FDA UDI 9865d8ca-1677-42d1-890e-8c6f7e1c4225 36 fields · synced Jun 8, 2026