← Back to catalogue

Fresnel Prism And Lens

FDA UDI

Class I (US FDA UDI)

by Fresnel Prism & Lens Co.

Identity

Trade Name
FRESNEL PRISM AND LENS FDA UDI
Generic Name
Trial lens set FDA UDI
Device Name
TRIAL RING - 2 DIOPTER NO HANDLE FDA UDI
Model / Reference
4000-2NH FDA UDI
Description
TRIAL RING - 2 DIOPTER NO HANDLE FDA UDI

Identifiers

Catalog Number
4000-2NH FDA UDI
Primary DI / UDI-DI
00850029104278 FDA UDI
FDA Product Code
HPC FDA UDI
GMDN Term
Trial lens set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1405 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Trial lens set

Fresnel Prism And Lens by Fresnel Prism & Lens Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trial lens set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 4406ea9e-9359-42b5-83d7-8186ade7bb73 35 fields · synced May 30, 2026