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IPC™ Visao®

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
IPC™ Visao® FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
IRR TUBING 3318603 IPC VISAO BUR GRD RC FDA UDI
Model / Reference
3318603 FDA UDI
Description
IRR TUBING 3318603 IPC VISAO BUR GRD RC FDA UDI

Identifiers

Primary DI / UDI-DI
00613994436382 FDA UDI
510(k) Number
K081277 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

IPC™ Visao® 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 2abd9637-0ad8-4aee-8cc3-758de5216199 35 fields · synced May 30, 2026