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ulrich medical disposables

FDA UDI

Class II (US FDA UDI)

by Ulrich GmbH & Co. KG

Identity

Trade Name
ulrich medical disposables FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
Patient tubing without RFID, 320 cm for ulricheasyINJECT CT/MRI injectors FDA UDI
Model / Reference
XD 10752 FDA UDI
Description
Patient tubing without RFID, 320 cm for ulricheasyINJECT CT/MRI injectors FDA UDI

Identifiers

Primary DI / UDI-DI
04052536203857 FDA UDI
510(k) Number
K233737 FDA UDI
K241850 FDA UDI
FDA Product Code
IZQ FDA UDI
GMDN Term
Electric infusion pump administration set, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric infusion pump administration set, single-use

ulrich medical disposables by Ulrich GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric infusion pump administration set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b0ef23aa-1cb1-40c3-8605-800610fd8331 34 fields · synced Jun 1, 2026