Bausch + Lomb

FDA UDI

Class I (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name: Bausch + Lomb FDA UDI
Generic Name: Corneal scissors, reusable FDA UDI
Device Name: SCISSORS BECKER FDA UDI
Model / Reference: N3090 FDA UDI
Description: SCISSORS BECKER FDA UDI

Identifiers

Catalog Number: N3090 FDA UDI
Primary DI / UDI-DI: 00757770418084 FDA UDI
FDA Product Code: KBD FDA UDI
GMDN Term: Corneal scissors, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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

Yes

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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Corneal scissors, reusable

Bausch + Lomb by Bausch & Lomb Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Corneal scissors, reusable.

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RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
Stephens Instruments — KRISHNA IMPORTS INC · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Ophthalmic Scissors — Katena Products, Inc. · 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: Bausch & Lomb Incorporated

Sources (1)

FDA UDI 7c590bb9-8b87-4067-b012-d31d4e59321c 34 fields · synced Jun 8, 2026