← Back to catalogue

Ophthalmic Scissors

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Ophthalmic Scissors FDA UDI
Generic Name
Corneal scissors, reusable FDA UDI
Device Name
CASTROVIEJO CORNEOSCLERAL SCISSORS SM RT FDA UDI
Model / Reference
K4-1000 FDA UDI
Description
CASTROVIEJO CORNEOSCLERAL SCISSORS SM RT FDA UDI

Identifiers

Catalog Number
K4-1000 FDA UDI
Primary DI / UDI-DI
00841668105054 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Corneal scissors, 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: Corneal scissors, reusable

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

Similar devices

Also classified as Corneal scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 570aae37-6266-4314-bfd2-afe6ba2070f9 35 fields · synced Jun 12, 2026