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Oph.Forceps

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Oph.Forceps FDA UDI
Generic Name
Eyelid clamp, reusable FDA UDI
Device Name
Francis Chalazion Forceps, 12x14mm FDA UDI
Model / Reference
08-01715 FDA UDI
Description
Francis Chalazion Forceps, 12x14mm FDA UDI

Identifiers

Catalog Number
08-01715 FDA UDI
Primary DI / UDI-DI
00841668118177 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Eyelid clamp, 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

Dimensions & Sizes

Size
Length — 12 Millimeter FDA UDI
Width — 14 Millimeter FDA UDI

Category: Eyelid clamp, reusable

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

Similar devices

Also classified as Eyelid clamp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ae8b8f1-8848-4ffb-9f8b-89d27540cd95 36 fields · synced Jun 12, 2026