Crosswalk

FDA UDI

Class II (US FDA UDI)

by Asahi Intecc Co., Ltd.

Identity

Trade Name: CROSSWALK FDA UDI
Generic Name: Vascular microcatheter FDA UDI
Model / Reference: PSC14135C FDA UDI

Identifiers

Primary DI / UDI-DI: 04547327133715 FDA UDI
FDA Product Code: DQY FDA UDI
GMDN Term: Vascular microcatheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1250 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 2.2 French FDA UDI
Length — 135 Centimeter FDA UDI

Category: Vascular microcatheter

Crosswalk by Asahi Intecc Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Renegade™ HI-FLO™ Kit — Boston Scientific · Class II
PROWLER — Medos International Sàrl · Class II
Merit Maestro® — Merit Medical Systems, Inc. · Class II
Lantern Delivery Catheter — PENUMBRA, INC. · Class II
Direxion™ Fathom™-16 System — Boston Scientific · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Asahi Intecc Co., Ltd.

Sources (1)

FDA UDI 31efb879-bb1c-4d4d-aa26-4989b44719f0 33 fields · synced Jun 6, 2026