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Ratchet Compressor

EUDAMED

Class I (EU MDR)

Ref 459800722203

by Philips Medical Systems Nederland B.V.

Identity

Trade Name
Ratchet Compressor EUDAMED
Device Name
Patient support accessories EUDAMED
Model / Reference
459800722203 EUDAMED

Identifiers

Primary DI / UDI-DI
00884838117150 EUDAMED
Basic UDI-DI
0884838BM798U8 EUDAMED
Direct Marketing DI
00884838117150 EUDAMED
EMDN Code
Z11030102 STATIONARY ANGIOGRAPHY SYSTEMS FOR ANGIOGRAPHIC AND CARDIOLOGIC STUDIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

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

Ratchet Compressor by Philips Medical Systems Nederland B.V. — Class I — 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

EUDAMED SRN
NL-MF-000001489

Sources (1)

  • EUDAMED ecd75522-8411-4ac0-b023-a2fe2356d345 61 fields · synced Oct 6, 2026