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SUPER VIEW® Pack

FDA UDI

Class II (US FDA UDI)

by Oculus Surgical Inc

Identity

Trade Name
SUPER VIEW® Pack FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
1 Each 40411 Sterile Disposable SUPER VIEW® Lens Set & 1 Each 40100 Sterile Microscope Drape FDA UDI
Model / Reference
40211 FDA UDI
Description
1 Each 40411 Sterile Disposable SUPER VIEW® Lens Set & 1 Each 40100 Sterile Microscope Drape FDA UDI

Identifiers

Catalog Number
40211 FDA UDI
Primary DI / UDI-DI
00856222004025 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 13 Millimeter FDA UDI
Outer Diameter — 18 Millimeter FDA UDI
Outer Diameter — 42 Millimeter FDA UDI

Category: Medical equipment/instrument drape, single-useOphthalmic diagnostic condensing lensVitrectomy contact lens, single-use

SUPER VIEW® Pack by Oculus Surgical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy contact lens, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oculus Surgical Inc

Sources (1)

  • FDA UDI b2865edd-599e-4b0a-86ec-7087560dc1b7 37 fields · synced May 30, 2026