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Vial Assembly

FDA UDI

Class II (US FDA UDI)

by Paragon Vision Sciences

Identity

Trade Name
Vial Assembly FDA UDI
Generic Name
Contact lens case FDA UDI
Device Name
Contact lens vial with cap and gasket/claw The finished assemblies can be made with variation in the color of the cap and the insertion of a gasket or a claw. Additionally, the claw has three distinct sizes, Small (S), Large (L), and Extra Large (X). FDA UDI
Model / Reference
900 FDA UDI
Description
Contact lens vial with cap and gasket/claw The finished assemblies can be made with variation in the color of the cap and the insertion of a gasket or a claw. Additionally, the claw has three distinct sizes, Small (S), Large (L), and Extra Large (X). FDA UDI

Identifiers

Primary DI / UDI-DI
B222900 FDA UDI
FDA Product Code
LRX FDA UDI
GMDN Term
Contact lens case FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.5928 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Contact lens case

Vial Assembly by Paragon Vision Sciences — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contact lens case.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 97ac2c69-18c6-4c08-9827-8a56dc50ef21 33 fields · synced Jun 6, 2026