Identity
- Trade Name
- CR HD5.0 AEC CASSETTE FDA UDI
- Generic Name
- Digital imaging cassette FDA UDI
- Device Name
- CR HD5.0 AEC CASSETTE 24X30CM FDA UDI
- Model / Reference
- CR HD5.0 AEC CASSETTE 24X30 FDA UDI
- Description
- CR HD5.0 AEC CASSETTE 24X30CM FDA UDI
Identifiers
- Catalog Number
- 5PCSZ FDA UDI
- Primary DI / UDI-DI
- 05414904044162 FDA UDI
- 510(k) Number
- K111324 FDA UDI
- FDA Product Code
- MUE FDA UDI
- GMDN Term
- Digital imaging cassette FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1715 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Width — 30 Centimeter FDA UDILength — 24 Centimeter FDA UDI
Category: Digital imaging cassette
Cr Hd5.0 Aec Cassette by Agfa Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K111324 also covers:
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
- Agfa Corp.
Sources (1)
- FDA UDI 9ef5592a-0c9a-476d-bd74-9627749829f2 37 fields · synced Jun 6, 2026