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ClearVu 2.7 Sharp

FDA UDI

Class I (US FDA UDI)

by Cannuflow, Inc.

Identity

Trade Name
ClearVu 2.7 Sharp FDA UDI
Generic Name
Arthroscopic access cannula, single-use FDA UDI
Device Name
Flexible Inflow-Outflow Cannula FDA UDI
Model / Reference
CV27-S FDA UDI
Description
Flexible Inflow-Outflow Cannula FDA UDI

Identifiers

Catalog Number
CV27-S FDA UDI
Primary DI / UDI-DI
00866497000318 FDA UDI
FDA Product Code
FGY FDA UDI
GMDN Term
Arthroscopic access cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 2.7 Millimeter FDA UDI

Category: Arthroscopic access cannula, single-use

ClearVu 2.7 Sharp by Cannuflow, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cannuflow, Inc.

Sources (1)

  • FDA UDI a7923fb5-3511-425c-8edb-2b74221c9dd4 35 fields · synced May 31, 2026