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Intellio Shift

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
INTELLIO SHIFT FDA UDI
Generic Name
Electrosurgical system generator FDA UDI
Device Name
NEO CONTROLLER REFURBISH FDA UDI
Model / Reference
72290150F FDA UDI
Description
NEO CONTROLLER REFURBISH FDA UDI

Identifiers

Catalog Number
72290150F FDA UDI
Primary DI / UDI-DI
00885556902738 FDA UDI
510(k) Number
K232290 FDA UDI
FDA Product Code
HRX FDA UDI
GEI FDA UDI
GMDN Term
Electrosurgical system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical system generator

Intellio Shift by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system generator.

Cleared under the same submission

K232290 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 2861923d-d4fd-4b32-bafb-18f693d5e57c 36 fields · synced Jun 8, 2026