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CannulaCRF

FDA UDI

Class II (US FDA UDI)

by Cambridge Interventional LLC

Identity

Trade Name
CannulaCRF FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI
Device Name
CRF Radiofrequency Cannula FDA UDI
Model / Reference
CRF-C2007 FDA UDI
Description
CRF Radiofrequency Cannula FDA UDI

Identifiers

Catalog Number
CRF-C2007 FDA UDI
Primary DI / UDI-DI
00811746030899 FDA UDI
510(k) Number
K192715 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe cannula, single-use 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

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: Percutaneous radio-frequency ablation probe cannula, single-use

CannulaCRF by Cambridge Interventional LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe cannula, single-use.

Cleared under the same submission

K192715 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cambridge Interventional LLC

Sources (1)

  • FDA UDI 62aed768-5bf0-4dde-8d68-cf7edd1a6b55 37 fields · synced Jun 8, 2026