Identity
- Trade Name
- PuriLens Plus Disinfecting System Exchange Kit FDA UDI
- Generic Name
- Contact lens agitation cleaning system, mechanical FDA UDI
- Device Name
- Exchange Kit contents: PuriLens Unit and removable cleaning/disinfecting chamber. FDA UDI
- Model / Reference
- MS0610/H FDA UDI
- Description
- Exchange Kit contents: PuriLens Unit and removable cleaning/disinfecting chamber. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00830002000056 FDA UDI
- FDA Product Code
- LYL FDA UDI
- GMDN Term
- Contact lens agitation cleaning system, mechanical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 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
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
PuriLens Plus Disinfecting System Exchange Kit by Lifestyle Co Inc, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Lifestyle Co Inc, The
Sources (1)
- FDA UDI b2fd4811-f6bc-4398-b54c-93f3fa833f57 35 fields · synced May 30, 2026