Versa Optic Set, for f=175mm

FDA UDI

Class I (US FDA UDI)

by Oculus Surgical Inc

Identity

Trade Name: Versa Optic Set, for f=175mm FDA UDI
Generic Name: Ophthalmic diagnostic condensing lens FDA UDI
Device Name: 1 Versa Optic Set, for f=175mm FDA UDI
Model / Reference: 54211 FDA UDI
Description: 1 Versa Optic Set, for f=175mm FDA UDI

Identifiers

Catalog Number: 54211 FDA UDI
Primary DI / UDI-DI: 00852475007219 FDA UDI
FDA Product Code: HJL FDA UDI
GMDN Term: Ophthalmic diagnostic condensing lens FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.1380 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 12 Millimeter FDA UDI
Outer Diameter — 18 Millimeter FDA UDI

Category: Ophthalmic diagnostic condensing lens

Versa Optic Set, for f=175mm by Oculus Surgical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Oculus Surgical Inc

Sources (1)

FDA UDI 7dfdfbbd-d0f9-47ba-bfd2-3d7d60db0e09 37 fields · synced May 30, 2026