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3D X-Ray Tube mount

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
3D X-Ray Tube mount FDA UDI
Generic Name
Stationary basic diagnostic x-ray system, digital FDA UDI
Device Name
X-Ray Tube mount FDA UDI
Model / Reference
10501776 FDA UDI
Description
X-Ray Tube mount FDA UDI

Identifiers

Primary DI / UDI-DI
04056869025209 FDA UDI
FDA Product Code
IYB FDA UDI
GMDN Term
Stationary basic diagnostic x-ray system, digital FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1770 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stationary basic diagnostic x-ray system, digital

3D X-Ray Tube mount by Siemens Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare

Sources (1)

  • FDA UDI b51fe34a-0a27-4ad3-8c90-7a4df9808633 34 fields · synced Jun 8, 2026