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IntraVu Scope 120

FDA UDI

Class II (US FDA UDI)

by Intravu, Inc.

Identity

Trade Name
IntraVu Scope 120 FDA UDI
Generic Name
Rigid optical arthroscope, single-use FDA UDI
Device Name
Kit containing 120mm Scope and 120mm Cannula, 120mm Trocar, and Stopcock. IntraVu Scope is a miniaturized, sterile, single-use disposable scope for use with the IntraVu Tablet reusable video processing unit. FDA UDI
Model / Reference
IV-ASY-1120 FDA UDI
Description
Kit containing 120mm Scope and 120mm Cannula, 120mm Trocar, and Stopcock. IntraVu Scope is a miniaturized, sterile, single-use disposable scope for use with the IntraVu Tablet reusable video processing unit. FDA UDI

Identifiers

Catalog Number
IV-ASY-1120 FDA UDI
Primary DI / UDI-DI
00865351000341 FDA UDI
510(k) Number
K181982 FDA UDI
FDA Product Code
HRX FDA UDI
GCJ FDA UDI
GMDN Term
Rigid optical arthroscope, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
876.1500 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 120 Millimeter FDA UDI

Category: Rigid optical arthroscope, single-use

IntraVu Scope 120 by Intravu, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical arthroscope, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intravu, Inc.

Sources (1)

  • FDA UDI 51f83d38-138c-47c0-ac4e-4c597626306b 38 fields · synced May 30, 2026