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Carpediem

FDA UDI

Class II (US FDA UDI)

by Mozarc Medical US LLC

Identity

Trade Name
CARPEDIEM FDA UDI
Generic Name
Haemodialysis/haemofiltration system component set FDA UDI
Device Name
BL 250 HEMOFILTRATION/HEMODIALYSIS KIT 025 FOR CARPEDIEM FDA UDI
Model / Reference
IB0595580 FDA UDI
Description
BL 250 HEMOFILTRATION/HEMODIALYSIS KIT 025 FOR CARPEDIEM FDA UDI

Identifiers

Primary DI / UDI-DI
08032979792299 FDA UDI
FDA Product Code
QIR FDA UDI
GMDN Term
Haemodialysis/haemofiltration system component set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5861 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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

No

FDA UDI

Category: Haemodialysis/haemofiltration system component set

Carpediem by Mozarc Medical US LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis/haemofiltration system component set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mozarc Medical US LLC

Sources (1)

  • FDA UDI 5be88ebf-0b95-410c-a828-ba8cb5df328d 36 fields · synced Jun 8, 2026