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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
General surgery wound probe/packer FDA UDI
Device Name
ECONO STERILE PROBE W/EYE TRAY CS/50 FDA UDI
Model / Reference
94-5923 FDA UDI
Description
ECONO STERILE PROBE W/EYE TRAY CS/50 FDA UDI

Identifiers

Primary DI / UDI-DI
10649111181665 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
General surgery wound probe/packer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: General surgery wound probe/packer

Sklar Instruments by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgery wound probe/packer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 12026791-a432-489c-b39c-3440242e448e 33 fields · synced May 30, 2026