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Sklar Instruments

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar Instruments FDA UDI
Generic Name
Eye muscle hook, reusable FDA UDI
Device Name
ECONO STERILE IRIS HOOK QK REL 4MM 9" STER25 FDA UDI
Model / Reference
96-2224A FDA UDI
Description
ECONO STERILE IRIS HOOK QK REL 4MM 9" STER25 FDA UDI

Identifiers

Primary DI / UDI-DI
10649111487934 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Eye muscle hook, reusable

Sklar Instruments by Sklar Corporation — 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

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 5aef096c-c34f-4ac7-bef0-1bbd9998b5f5 33 fields · synced May 30, 2026