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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
PSC35150S FDA UDI

Identifiers

Primary DI / UDI-DI
04547327133579 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

No

FDA UDI

Contains Latex

No

FDA UDI

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
Catheter Gauge — 4.2 French FDA UDI
Length — 150 Centimeter FDA UDI

Category: Vascular microcatheter

For medical professionals and patients, the CROSSWALK vascular microcatheter provides precise control over fluid infusion into small vessels for diagnostic or therapeutic purposes. This single-use device is designed for minimally invasive procedures, offering a flexible and effective solution for various vascular conditions.

Similar devices

Also classified as Vascular microcatheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asahi Intecc Co., Ltd.

Sources (1)

  • FDA UDI f0bbb989-9f51-46d9-a2b5-4f9ba1a60170 33 fields · synced Jun 28, 2026