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Rexall Contact Lens Case

FDA UDI

Class II (US FDA UDI)

by Shanghai Care US Medical Product Co., Ltd.

Identity

Trade Name
Rexall Contact Lens Case FDA UDI
Generic Name
Contact lens case FDA UDI
Model / Reference
A0373 FDA UDI

Identifiers

Primary DI / UDI-DI
06970285515671 FDA UDI
510(k) Number
K160005 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Contact lens case

Rexall Contact Lens Case by Shanghai Care US Medical Product Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contact lens case.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b474e49d-bc9d-49a3-b49f-7bd449f535a7 33 fields · synced May 30, 2026