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Artis zee floor

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
Artis zee floor FDA UDI
Generic Name
Stationary angiographic x-ray system, digital FDA UDI
Model / Reference
10094135 FDA UDI

Identifiers

Primary DI / UDI-DI
04056869010045 FDA UDI
510(k) Number
K122644 FDA UDI
K141574 FDA UDI
K181407 FDA UDI
FDA Product Code
JAK FDA UDI
OWB FDA UDI
IZI FDA UDI
JAA FDA UDI
GMDN Term
Stationary angiographic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
892.1650 FDA UDI
892.1600 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

No

FDA UDI

Category: Stationary angiographic x-ray system, digital

Artis zee floor by Siemens Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary angiographic x-ray system, digital.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare

Sources (1)

  • FDA UDI 2e6770d4-088f-4aaa-b4e1-c5a21f4b2677 35 fields · synced Jun 1, 2026