Identity
- Trade Name
- AWS-h FDA UDI
- Generic Name
- Stationary mammographic x-ray system, digital FDA UDI
- Device Name
- FDR-3000AWS is a workstation used for Mammography System, intended to associate digital mammography images with patient and exam information, apply image processing to facilitate diagnosis, display the image, and output the resulting image and exam data for further display, distribution, or archiving. FDA UDI
- Model / Reference
- FDR-3000AWS FDA UDI
- Description
- FDR-3000AWS is a workstation used for Mammography System, intended to associate digital mammography images with patient and exam information, apply image processing to facilitate diagnosis, display the image, and output the resulting image and exam data for further display, distribution, or archiving. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04547410316902 FDA UDI
- 510(k) Number
- K133972 FDA UDI
- FDA Product Code
- MUE FDA UDI
- GMDN Term
- Stationary mammographic x-ray system, digital 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
No
FDA UDI
Category: Stationary mammographic x-ray system, digital
AWS-h by FUJIFILM Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K133972 also covers:
- 18x24 Compression plate (High) — FUJIFILM Corporation
- 18x24 Compression plate (Low) — FUJIFILM Corporation
- 18x24 Spot compression plate — FUJIFILM Corporation
- 18x24 comfort paddle (FS Small) — FUJIFILM Corporation
- 18x24 compression plate (Small) — FUJIFILM Corporation
- 18x24L comfort paddle (FS) — FUJIFILM Corporation
- 18x24L compression plate (Flex) — FUJIFILM Corporation
- 1Shot Phantom M Plus 24x30 — FUJIFILM Corporation
- 24x30 Compression plate (High) — FUJIFILM Corporation
- 24x30 Compression plate (Low) — FUJIFILM Corporation
- 24x30 compression plate (Shift Small) — FUJIFILM Corporation
- 24x30 compression plate (Shift) — FUJIFILM Corporation
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
- FUJIFILM Corporation
Sources (1)
- FDA UDI 5fb43552-91f7-4e09-bb1a-9411bf40d87f 35 fields · synced May 30, 2026