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Up & Up

FDA UDI

Class II (US FDA UDI)

by Target Corporation

Identity

Trade Name
UP & UP FDA UDI
Generic Name
Contact lens case FDA UDI
Device Name
Contact Lens Case 1ct FDA UDI
Model / Reference
245090197 FDA UDI
Description
Contact Lens Case 1ct FDA UDI

Identifiers

Catalog Number
4188T FDA UDI
Primary DI / UDI-DI
00756063059263 FDA UDI
510(k) Number
K991206 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
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

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

Up & Up by Target Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K991206 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI 14cdba29-789e-48a8-82e5-7475e4f4b97e 36 fields · synced May 30, 2026