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EndoCATH

FDA UDI

Class II (US FDA UDI)

by Sentreheart, Inc

Identity

Trade Name
EndoCATH FDA UDI
Generic Name
Intravascular occluding balloon catheter, image-guided FDA UDI
Device Name
Large Occlusion Balloon Catheter FDA UDI
Model / Reference
2006 FDA UDI
Description
Large Occlusion Balloon Catheter FDA UDI

Identifiers

Catalog Number
2006 FDA UDI
Primary DI / UDI-DI
M95520060 FDA UDI
510(k) Number
K070126 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Intravascular occluding balloon catheter, image-guided 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

Category: Intravascular occluding balloon catheter, image-guided

EndoCATH by Sentreheart, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular occluding balloon catheter, image-guided.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sentreheart, Inc

Sources (1)

  • FDA UDI be0cb07a-c564-4c72-8e2c-ee60389c889c 36 fields · synced May 30, 2026