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Ophthalmic cannula

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Ophthalmic cannula FDA UDI
Generic Name
Ophthalmic needle, single-use FDA UDI
Device Name
23g x 7/8" Atkinson, Peribulbar, 10/Box FDA UDI
Model / Reference
07-4023 FDA UDI
Description
23g x 7/8" Atkinson, Peribulbar, 10/Box FDA UDI

Identifiers

Catalog Number
07-4023 FDA UDI
Primary DI / UDI-DI
00841668117293 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Ophthalmic needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Length — 0.875 Inch FDA UDI
Needle Gauge — 23 Gauge FDA UDI

Category: Ophthalmic needle, single-use

Ophthalmic cannula by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d8228e49-5ce2-448f-8d46-09124efe0742 36 fields · synced Jun 12, 2026