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AcQGuide VUE

FDA UDI

Class II (US FDA UDI)

by Acutus Medical, Inc.

Identity

Trade Name
AcQGuide VUE FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
AcQGuide VUE Steerable Sheath FDA UDI
Model / Reference
900201 FDA UDI
Description
AcQGuide VUE Steerable Sheath FDA UDI

Identifiers

Catalog Number
900201 FDA UDI
Primary DI / UDI-DI
00857042007906 FDA UDI
FDA Product Code
DRA FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1280 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

Category: Vascular guide-catheter, single-use

AcQGuide VUE by Acutus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular guide-catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acutus Medical, Inc.

Sources (1)

  • FDA UDI 4b85e5c9-f0a4-41cf-ba5d-573104d7c98f 35 fields · synced May 30, 2026