← Back to catalogue

CozyTherm Heat Relief Patch, Neck

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
CozyTherm Heat Relief Patch, Neck FDA UDI
Generic Name
Exothermic heat therapy pack/patch FDA UDI
Model / Reference
1458 FDA UDI

Identifiers

Primary DI / UDI-DI
00840117341067 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Exothermic heat therapy pack/patch

CozyTherm Heat Relief Patch, Neck by Dynarex Corp. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 91b2df61-3fab-4659-8f70-c3a9a34783dd 32 fields · synced May 30, 2026