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Intelliflow™

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Intelliflow™ FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
CONTROL IRD200 IPC IRRIGATION REMOTE FDA UDI
Model / Reference
IRD200 FDA UDI
Description
CONTROL IRD200 IPC IRRIGATION REMOTE FDA UDI

Identifiers

Primary DI / UDI-DI
00613994384034 FDA UDI
510(k) Number
K081475 FDA UDI
FDA Product Code
HBE FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4310 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation tubing set, single-use

Intelliflow™ by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66eab1bf-927c-4dd0-9d1e-418f45c89233 35 fields · synced May 31, 2026