SUPER VIEW® Disposable Lens Set, Pivot

FDA UDI

Class I (US FDA UDI)

by Oculus Surgical Inc

Identity

Trade Name: SUPER VIEW® Disposable Lens Set, Pivot FDA UDI
Generic Name: Ophthalmic diagnostic condensing lens FDA UDI
Device Name: 1 Each SUPER VIEW® Sterile Disposable Pivot Lens Set for use with the SUPER VIEW® System or BIOM® FDA UDI
Model / Reference: 40223 FDA UDI
Description: 1 Each SUPER VIEW® Sterile Disposable Pivot Lens Set for use with the SUPER VIEW® System or BIOM® FDA UDI

Identifiers

Catalog Number: 40223 FDA UDI
Primary DI / UDI-DI: 00856222004742 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: Outer Diameter — 18 Millimeter FDA UDI
Outer Diameter — 42 Millimeter FDA UDI

Category: Ophthalmic diagnostic condensing lens

SUPER VIEW® Disposable Lens Set, Pivot by Oculus Surgical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic diagnostic condensing lens.

SuperField® NC — VOLK OPTICAL INC. · Class I
20D Large Clear, Red Ring — VOLK OPTICAL INC. · Class I
78D Limited Edition — VOLK OPTICAL INC. · Class I
28D Limited Edition — VOLK OPTICAL INC. · Class I
Primary Lens Set, 28D, 90D, 3 Mirror — Katena Products, Inc. · Class I
Super VitreoFundus® — VOLK OPTICAL INC. · Class I
78D Clear, Custom Color Ring — VOLK OPTICAL INC. · Class I
90D Clear, Green Ring — VOLK OPTICAL 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Oculus Surgical Inc

Sources (1)

FDA UDI 79639c72-71b2-4489-a0f5-7047e3545376 37 fields · synced May 31, 2026