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Super View® Lens Set, Disposable, Pivot, for BIOM ml/cl

FDA UDI

Class I (US FDA UDI)

by Oculus Surgical Inc

Identity

Trade Name
Super View® Lens Set, Disposable, Pivot, for BIOM ml/cl FDA UDI
Generic Name
Ophthalmic diagnostic condensing lens FDA UDI
Device Name
1 Each Super View® Sterile Disposable Pivot Lens Sets for use with the BIOM® ml/cl FDA UDI
Model / Reference
54014 FDA UDI
Description
1 Each Super View® Sterile Disposable Pivot Lens Sets for use with the BIOM® ml/cl FDA UDI

Identifiers

Catalog Number
54014 FDA UDI
Primary DI / UDI-DI
00852475007189 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Category: Ophthalmic diagnostic condensing lens

Super View® Lens Set, Disposable, Pivot, for BIOM ml/cl 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.

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 15fe4c80-80c3-4215-b3ed-707525dc11a7 36 fields · synced May 30, 2026