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Trocar set 23G with removable valve

FDA UDI

Class I (US FDA UDI)

by Aktive Srl

Identity

Trade Name
Trocar set 23G with removable valve FDA UDI
Generic Name
Ophthalmic working-channel cannula, single-use FDA UDI
Device Name
Trocar set 23G with removable valve FDA UDI
Model / Reference
AK-0350/N FDA UDI
Description
Trocar set 23G with removable valve FDA UDI

Identifiers

Catalog Number
AK-0350/N FDA UDI
Primary DI / UDI-DI
08052276019615 FDA UDI
FDA Product Code
NGY FDA UDI
GMDN Term
Ophthalmic working-channel cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic working-channel cannula, single-use

Trocar set 23G with removable valve by Aktive Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic working-channel cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aktive Srl

Sources (1)

  • FDA UDI c1f0051c-3d3e-4faf-909c-e133b00ae398 36 fields · synced May 30, 2026