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Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
WALGREENS FDA UDI
Generic Name
Knee/ankle/foot orthosis FDA UDI
Device Name
WALG STIRRUP ANKLE BRACE W/HT&CLD PADS FDA UDI
Model / Reference
871055 FDA UDI
Description
WALG STIRRUP ANKLE BRACE W/HT&CLD PADS FDA UDI

Identifiers

Primary DI / UDI-DI
00049022176409 FDA UDI
FDA Product Code
ITW FDA UDI
IME FDA UDI
GMDN Term
Knee/ankle/foot orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 FDA UDI
890.5700 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hot/cold therapy pack, reusableKnee/ankle/foot orthosis

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

Similar devices

Also classified as Knee/ankle/foot orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 5d835a96-6b63-47a6-9c9a-7c41f5b7015c 33 fields · synced Jun 8, 2026