Bausch + Lomb

FDA UDI

Class I (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name: Bausch + Lomb FDA UDI
Generic Name: Flieringa ophthalmic ring FDA UDI
Device Name: RNG SCLERAL BLEP MCNEIL-GOLDMN FDA UDI
Model / Reference: E4033 FDA UDI
Description: RNG SCLERAL BLEP MCNEIL-GOLDMN FDA UDI

Identifiers

Catalog Number: E4033 FDA UDI
Primary DI / UDI-DI: 00757770418855 FDA UDI
FDA Product Code: HNH FDA UDI
GMDN Term: Flieringa ophthalmic ring 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

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

Category: Flieringa ophthalmic ring

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

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Symmetry Flieringa — SYMMETRY SURGICAL INC. · Class I
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V. Mueller — STERIS CORPORATION · 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 7e45babd-ef9b-4c4e-8ef0-31f6bb67e506 34 fields · synced Jun 8, 2026