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Quikdraw Pro, White, X-Large

EUDAMED

Class I (EU MDR)

Ref 993040

by Aspen Medical Products, LLC

Identity

Trade Name
QUIKDRAW PRO, WHITE, X-LARGE EUDAMED
Device Name
LUMBAR EUDAMED
Model / Reference
993040 EUDAMED

Identifiers

Primary DI / UDI-DI
00818249011059 EUDAMED
Basic UDI-DI
081824901LSOH8 EUDAMED
EMDN Code
Y060308 LUMBOSACRAL SPINE ORTHOSES 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

Quikdraw Pro, White, X-Large by Aspen Medical Products, LLC — 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
US-MF-000001571
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 0bb2cb71-b336-4756-b8da-6301251bf13a 61 fields · synced Jun 19, 2026