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ASAHI Gladius MG14 190cm Pre-shape

EUDAMEDFDA UDI

Class III (EU MDR)

Ref AP14R023P

by Asahi Intecc Co., Ltd.

Identity

Trade Name
ASAHI Gladius MG14 190cm Pre-shape EUDAMED
ASAHI Gladius Mongo14 FDA UDI
Generic Name
Cardiac/peripheral vascular guidewire, single-use FDA UDI
Device Name
ASAHI PTCA Guide Wire ASAHI Gladius EUDAMED
Model / Reference
AP14R023P EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04547327123693 EUDAMEDFDA UDI
Basic UDI-DI
B-04547327123693 EUDAMED
FDA Product Code
DQX FDA UDI
EMDN Code
C04030201 INTERVENTIONAL 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
Austria 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

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

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

Dimensions & Sizes

Size
Length — 190 Centimeter FDA UDI
Outer Diameter — 0.014 Inch FDA UDI

ASAHI Gladius MG14 190cm Pre-shape by Asahi Intecc Co., Ltd. — 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
JP-MF-000010199
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED fc4b47a7-8ca9-444e-aae3-e64af5962bbe 61 fields · synced Jun 18, 2026
  • FDA UDI 4c313a89-e9d9-4e6f-93a1-77858e5d7d21 33 fields · synced May 30, 2026