Identity
- Trade Name
- Senographe Pristina FDA UDI
- Generic Name
- Stationary mammographic x-ray system, digital FDA UDI
- Device Name
- Senographe Pristina 3D UDI FDA UDI
- Model / Reference
- NAY3 FDA UDI
- Description
- Senographe Pristina 3D UDI FDA UDI
Identifiers
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Stationary mammographic x-ray system, digital
Senographe Pristina by Ge Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K162268 also covers:
- MagStand 1.5 — GE MEDICAL SYSTEMS, INC.
- MagStand 1.8 — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
- Pristina Paddle — GE MEDICAL SYSTEMS, INC.
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
- Ge Medical Systems, Inc.
Sources (1)
- FDA UDI df8e3e9b-9d64-469e-8ec5-9e9b64e1c70f 35 fields · synced Jun 8, 2026