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Ilp Ht Lf

EUDAMED

Class IIa (EU MDR)

Ref R9900129Model R9900086

by Rand S.p.A.

Identity

Trade Name
ILP HT LF EUDAMED
Device Name
ILP HT EUDAMED
Model / Reference
R9900086 EUDAMED
R9900129 EUDAMED

Identifiers

Primary DI / UDI-DI
+M640R99001291001 EUDAMED
Basic UDI-DI
++M640ILPX4 EUDAMED
EMDN Code
Z1204021585 MULTI-DISTRICT ONCOLOGICAL THERAPY INSTRUMENTS (EXCLUDING RADIOTHERAPY) - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ilp Ht Lf by Rand S.p.A. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Rand S.p.A.
EUDAMED SRN
IT-MF-000013507

Sources (1)

  • EUDAMED 18d48f41-4ab3-461a-943f-84601ac8cf97 61 fields · synced Jul 20, 2026