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Aristotle 24 Guidewire

EUDAMEDFDA UDI

Class III (EU MDR)

Ref A24-200-001Model 00896

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-Soft FDA UDI
Model / Reference
00896 EUDAMED
A24-200-001 EUDAMED
24-200-001 FDA UDI
Description
Guidewire-Soft FDA UDI

Identifiers

Catalog Number
A24-200-001 FDA UDI
Primary DI / UDI-DI
00818075010127 EUDAMEDFDA UDI
Basic UDI-DI
B-00818075010127 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 4c0e7b88-5fef-41d5-b457-8ea047c67433 61 fields · synced Sep 18, 2026
  • FDA UDI e9ec58a6-0287-4b62-952a-d03b7f734b9a 37 fields · synced May 30, 2026