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Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Exothermic heat therapy pack/patch FDA UDI
Device Name
Full Adhesive Heat Wraps Neck, Shoulder & Wrist FDA UDI
Model / Reference
993095 FDA UDI
Description
Full Adhesive Heat Wraps Neck, Shoulder & Wrist FDA UDI

Identifiers

Primary DI / UDI-DI
00311917194073 FDA UDI
FDA Product Code
OMW FDA UDI
GMDN Term
Exothermic heat therapy pack/patch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5710 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

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: Exothermic heat therapy pack/patch

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

Similar devices

Also classified as Exothermic heat therapy pack/patch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 3296a4a9-5836-40f1-a86a-cc6855316db3 34 fields · synced Jun 1, 2026