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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI
Device Name
Walgreens 3 Layer Earloop Mask, Black, 50 ct FDA UDI
Model / Reference
797626 FDA UDI
Description
Walgreens 3 Layer Earloop Mask, Black, 50 ct FDA UDI

Identifiers

Primary DI / UDI-DI
00311917057026 FDA UDI
510(k) Number
K213450 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/medical respirator, non-antimicrobial, single-use

Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical respirator, non-antimicrobial, single-use.

Cleared under the same submission

K213450 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 6169b42f-e247-4f93-9e5d-dca4a57cefb6 35 fields · synced May 30, 2026