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PuriLens Plus Disinfecting System Cleaning Chamber

FDA UDI

Class II (US FDA UDI)

by Lifestyle Co Inc, The

Identity

Trade Name
PuriLens Plus Disinfecting System Cleaning Chamber FDA UDI
Generic Name
Contact lens agitation cleaning system, mechanical FDA UDI
Device Name
Replacement cleaning chamber packaged in plastic zip-lock bag. FDA UDI
Model / Reference
MS0610/H FDA UDI
Description
Replacement cleaning chamber packaged in plastic zip-lock bag. FDA UDI

Identifiers

Primary DI / UDI-DI
00830002000049 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

No

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 Cleaning Chamber 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

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Manufacturer

Sources (1)

  • FDA UDI 33ef0462-e211-4ad6-800a-4eca78d5790b 35 fields · synced Jun 1, 2026