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INT, Falcon Guide Wire

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref HGST355AFModel 0.018" , 0.025", 0.028", 0.032", 0.038"

by Shanghai Kindly Medical Instruments Co., Ltd.

Identity

Trade Name
INT,Falcon Guide Wire FDA UDI
Generic Name
Cardiac/peripheral vascular guidewire, single-use FDA UDI
Device Name
Guidewire EUDAMED
0.035"*260cm, hydrophilic coating, angled tip, stiff FDA UDI
Model / Reference
HGST355AF EUDAMEDFDA UDI
0.018" , 0.025", 0.028", 0.032", 0.038" EUDAMED
Description
0.035"*260cm, hydrophilic coating, angled tip, stiff FDA UDI

Identifiers

Primary DI / UDI-DI
06950900952746 EUDAMEDFDA UDI
Basic UDI-DI
69509009CEGWSG EUDAMED
510(k) Number
K180177 FDA UDI
FDA Product Code
DQX FDA UDI
EMDN Code
C04020101 PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, HYDROPHILIC EUDAMED
GMDN Term
Cardiac/peripheral vascular guidewire, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.1330 FDA UDI
Market of Registration
Greece 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

No

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

Yes

FDA UDI

Category: Cardiac/peripheral vascular guidewire, single-use

INT, Falcon Guide Wire by Shanghai Kindly Medical Instruments Co., Ltd. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac/peripheral vascular guidewire, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI ee2128e3-f291-4be6-a177-78cd7383ec5a 34 fields · synced Oct 7, 2026
  • EUDAMED ebb987d8-de8a-4f6d-a82e-5b04fca94060 61 fields · synced Oct 7, 2026