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
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Paragon Vision Sciences
Sources (1)
- FDA UDI 97ac2c69-18c6-4c08-9827-8a56dc50ef21 33 fields · synced Jun 6, 2026