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Aristotle 24 Guidewire

EUDAMEDFDA UDI

Class III (EU MDR)

Ref A24-200-003Model 00898

by Scientia Vascular, Inc.

Identity

Trade Name
Aristotle 24 Guidewire EUDAMED
Aristotle FDA UDI
Generic Name
Cardiac/peripheral vascular guidewire, single-use FDA UDI
Device Name
Aristotle 24 Guidewire EUDAMED
Guidewire-Support FDA UDI
Model / Reference
00898 EUDAMED
A24-200-003 EUDAMED
24-200-003 FDA UDI
Description
Guidewire-Support FDA UDI

Identifiers

Catalog Number
A24-200-003 FDA UDI
Primary DI / UDI-DI
00818075010141 EUDAMEDFDA UDI
Basic UDI-DI
B-00818075010141 EUDAMED
510(k) Number
K192783 FDA UDI
FDA Product Code
DQX FDA UDI
MOF FDA UDI
EMDN Code
C04030101 DIAGNOSTIC CORONARY AND PERIPHERAL VASCULAR GUIDE WIRES, HYDROPHILIC EUDAMED
GMDN Term
Cardiac/peripheral vascular guidewire, single-use FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
870.1330 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Aristotle 24 Guidewire by Scientia Vascular, Inc. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000018661
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 4d9fc2a6-227c-41db-980b-621b659d165f 61 fields · synced Jul 22, 2026
  • FDA UDI 3c0834bc-8611-4d6e-8023-8b06fdf320cf 37 fields · synced May 30, 2026