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Oph.Hook

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Oph.Hook FDA UDI
Generic Name
Eye muscle hook, reusable FDA UDI
Device Name
Von Graefe Strabismus Hook, Medium, 10mm FDA UDI
Model / Reference
08-04406 FDA UDI
Description
Von Graefe Strabismus Hook, Medium, 10mm FDA UDI

Identifiers

Catalog Number
08-04406 FDA UDI
Primary DI / UDI-DI
00841668118986 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Eye muscle hook, 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 — 10 Millimeter FDA UDI

Category: Eye muscle hook, reusable

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

Similar devices

Also classified as Eye muscle hook, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11aebe38-605a-4c85-89fe-a3b12da0ea94 36 fields · synced Jun 12, 2026