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Barraquer Iris Scissors

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
BARRAQUER IRIS SCISSORS FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Device Name
BARRAQUER IRIS SCISSORS FDA UDI
Model / Reference
AE-5220 FDA UDI
Description
BARRAQUER IRIS SCISSORS FDA UDI

Identifiers

Catalog Number
AE-5220 FDA UDI
Primary DI / UDI-DI
00841668136911 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, conventional-hinge, reusable 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intraocular scissors, conventional-hinge, reusable

Barraquer Iris Scissors by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors, conventional-hinge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katena Products, Inc.

Sources (1)

  • FDA UDI edfd0f75-41dd-40c8-8a69-18dc9f053729 35 fields · synced Jun 12, 2026