← Back to catalogue

Visualase

FDA UDI

Class I (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
Visualase FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
IV POLE 9735556 VISUALASE FDA UDI
Model / Reference
9735556 FDA UDI
Description
IV POLE 9735556 VISUALASE FDA UDI

Identifiers

Primary DI / UDI-DI
00643169590113 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Freestanding/bed-attached intravenous pole FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding/bed-attached intravenous pole

Visualase by Medtronic Navigation, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding/bed-attached intravenous pole.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1abc27eb-9220-4d6c-864c-cb51ce0b8e59 34 fields · synced May 29, 2026