Sklar

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name: Sklar FDA UDI
Generic Name: Ophthalmic strabismus scissors, reusable FDA UDI
Device Name: BONACCOLTO STRABISMUS FCP SMTH FDA UDI
Model / Reference: 66-6336 FDA UDI
Description: BONACCOLTO STRABISMUS FCP SMTH FDA UDI

Identifiers

Primary DI / UDI-DI: 10649111454738 FDA UDI
FDA Product Code: HNR FDA UDI
GMDN Term: Ophthalmic strabismus scissors, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Ophthalmic strabismus scissors, reusable

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

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RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
Gimmi — Gimmi GmbH · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Sklar Corporation

Sources (1)

FDA UDI dc591616-627b-493a-b417-21e8f87e2087 33 fields · synced Jun 1, 2026