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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 VEIN HOOK 2.5MM STERILE CS/25 FDA UDI
Model / Reference
96-4022M FDA UDI
Description
ECONO STERILE VEIN HOOK 2.5MM STERILE CS/25 FDA UDI

Identifiers

Primary DI / UDI-DI
10649111476372 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Eye muscle hook, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 dc556a86-e799-4197-afe2-f5efd4444553 33 fields · synced May 30, 2026