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Corneal Trephine

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Corneal Trephine FDA UDI
Generic Name
Corneal trephine, single-use FDA UDI
Device Name
BARRON VACUUM TREPHINE 7.0MM FDA UDI
Model / Reference
K20-2054 FDA UDI
Description
BARRON VACUUM TREPHINE 7.0MM FDA UDI

Identifiers

Catalog Number
K20-2054 FDA UDI
Primary DI / UDI-DI
00841668112472 FDA UDI
FDA Product Code
HRH FDA UDI
GMDN Term
Corneal trephine, 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

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
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 7 Millimeter FDA UDI

Category: Corneal trephine, single-use

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

Similar devices

Also classified as Corneal trephine, single-use.

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 d5d8495b-eae9-4021-8ab9-3fd81b8a43a7 36 fields · synced Jun 12, 2026