← Back to catalogue

ulricheasyINJECT Max

FDA UDI

Class II (US FDA UDI)

by Ulrich GmbH & Co. KG

Identity

Trade Name
ulricheasyINJECT Max FDA UDI
Generic Name
MRI contrast medium injection system, line-powered, mobile FDA UDI
Device Name
ulricheasyINJECT Max 2M FDA UDI
Model / Reference
XD 10140 FDA UDI
Description
ulricheasyINJECT Max 2M FDA UDI

Identifiers

Primary DI / UDI-DI
04052536205493 FDA UDI
510(k) Number
K233737 FDA UDI
K241850 FDA UDI
FDA Product Code
IZQ FDA UDI
GMDN Term
MRI contrast medium injection system, line-powered, mobile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: MRI contrast medium injection system, line-powered, mobile

ulricheasyINJECT Max by Ulrich GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as MRI contrast medium injection system, line-powered, mobile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI cfa30de7-5393-4b90-a141-19df2c9504e8 34 fields · synced Jun 6, 2026