Nimbus Probe Adapter Cable

FDA UDI

Class II (US FDA UDI)

by Stratus Medical LLC

Identity

Trade Name: Nimbus Probe Adapter Cable FDA UDI
Generic Name: Electrosurgical cable adaptor FDA UDI
Device Name: Reusable RF Intermediate Adapter Cable FDA UDI
Model / Reference: RPC-C FDA UDI
Description: Reusable RF Intermediate Adapter Cable FDA UDI

Identifiers

Primary DI / UDI-DI: 05060224332078 FDA UDI
510(k) Number: K090608 FDA UDI
FDA Product Code: GXI FDA UDI
GMDN Term: Electrosurgical cable adaptor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4725 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical cable adaptor

Nimbus Probe Adapter Cable by Stratus Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K090608 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Stratus Medical LLC

Sources (1)

FDA UDI 09703141-a0fb-45f8-88eb-0ec027c9f058 34 fields · synced May 30, 2026