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IntelliBlate Microwave Ablation System Mobile Cart

FDA UDI

Class II (US FDA UDI)

by Endocare, Inc.

Identity

Trade Name
IntelliBlate Microwave Ablation System Mobile Cart FDA UDI
Generic Name
Microwave ablation system FDA UDI
Device Name
Mobile cart only for IntelliBlate microwave ablation system FDA UDI
Model / Reference
IB-CART FDA UDI
Description
Mobile cart only for IntelliBlate microwave ablation system FDA UDI

Identifiers

Primary DI / UDI-DI
00810563022285 FDA UDI
510(k) Number
K240480 FDA UDI
FDA Product Code
NEY FDA UDI
GMDN Term
Microwave ablation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Microwave ablation system

IntelliBlate Microwave Ablation System Mobile Cart by Endocare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endocare, Inc.

Sources (1)

  • FDA UDI 6fdcc121-33d8-4dea-94e2-3ba81fff3e6a 34 fields · synced May 30, 2026