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AcQRate Dx Fixed Curve Catheter

FDA UDI

Class II (US FDA UDI)

by VascoMed GmbH

Identity

Trade Name
AcQRate Dx Fixed Curve Catheter FDA UDI
Generic Name
Cardiac mapping catheter, percutaneous, single-use FDA UDI
Model / Reference
5J 6F 5-5-5-280 mm FDA UDI

Identifiers

Catalog Number
460650 FDA UDI
Primary DI / UDI-DI
04260090928912 FDA UDI
510(k) Number
K201445 FDA UDI
FDA Product Code
DRF FDA UDI
GMDN Term
Cardiac mapping catheter, percutaneous, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1220 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: Cardiac mapping catheter, percutaneous, single-use

AcQRate Dx Fixed Curve Catheter by VascoMed GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac mapping catheter, percutaneous, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VascoMed GmbH

Sources (1)

  • FDA UDI 185f6102-208b-487a-ac52-6f5ce6099cb2 37 fields · synced May 29, 2026