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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Contact lens case FDA UDI
Device Name
WALG TWIST TOP CONTACT LENS CASE FDA UDI
Model / Reference
SC-206 FDA UDI
Description
WALG TWIST TOP CONTACT LENS CASE FDA UDI

Identifiers

Primary DI / UDI-DI
00311917186795 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
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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 8 Milliliter FDA UDI

Category: Contact lens case

Walgreens by Walgreen Co. — 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

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 0f0c5f80-df47-4126-86cd-c33eb3acafc5 36 fields · synced Jun 8, 2026