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Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Woven gauze roll/sheet FDA UDI
Device Name
Bandage Roll. 4.5 IN X 4 YARDS. FDA UDI
Model / Reference
344343 FDA UDI
Description
Bandage Roll. 4.5 IN X 4 YARDS. FDA UDI

Identifiers

Catalog Number
WRX344343V1 FDA UDI
Primary DI / UDI-DI
00311917166131 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze roll/sheet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze roll/sheet

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

Similar devices

Also classified as Woven gauze roll/sheet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 0b38c575-d2e5-414c-aee5-5657182347d8 35 fields · synced May 30, 2026