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Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear

FDA UDI

Class III (US FDA UDI)

by Euclid Vision Corporation

Identity

Trade Name
Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear FDA UDI
Generic Name
Orthokeratology contact lens FDA UDI
Device Name
Kit containing 850007135072 (Emerald Toric, opirfocon A, Blue) and 850007135089 (Emerald Toric, oprifocon A, Green) FDA UDI
Model / Reference
Emerald Toric FDA UDI
Description
Kit containing 850007135072 (Emerald Toric, opirfocon A, Blue) and 850007135089 (Emerald Toric, oprifocon A, Green) FDA UDI

Identifiers

Primary DI / UDI-DI
18500071350237 FDA UDI
FDA Product Code
NUU FDA UDI
GMDN Term
Orthokeratology contact lens FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.5916 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear by Euclid Vision Corporation — Class III — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e57910f4-6590-4c55-8e95-652fc7fac3d2 35 fields · synced Jun 8, 2026