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Crit-Line®

FDA UDI

Class II (US FDA UDI)

by Fresenius Usa, Inc.

Identity

Trade Name
Crit-Line® FDA UDI
Generic Name
Haemodialysis system blood volume monitor FDA UDI
Device Name
Viewing window for CLiC technology FDA UDI
Model / Reference
CL10041021 FDA UDI
Description
Viewing window for CLiC technology FDA UDI

Identifiers

Catalog Number
CL10041021 FDA UDI
Primary DI / UDI-DI
00840861100552 FDA UDI
FDA Product Code
KOC FDA UDI
GMDN Term
Haemodialysis system blood volume monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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

No

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

Yes

FDA UDI

Category: Haemodialysis system blood volume monitor

Crit-Line® by Fresenius Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis system blood volume monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fresenius Usa, Inc.

Sources (1)

  • FDA UDI 7edb415a-77e2-41aa-9d2f-e66f72137f02 36 fields · synced Jun 8, 2026