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Meijer Hot & Cold Therapy Wrap with Clay Based Technology

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer Hot & Cold Therapy Wrap with Clay Based Technology FDA UDI
Generic Name
Hot/cold therapy pack, reusable FDA UDI
Device Name
6" x 12" (15.24 cm x 30.48 cm) clay pack used along with soft cover equipped with elastic strap to relieve sore muscles, stiff muscles and joints, head and back aches, cramps and athletic injuries. FDA UDI
Model / Reference
3458398 FDA UDI
Description
6" x 12" (15.24 cm x 30.48 cm) clay pack used along with soft cover equipped with elastic strap to relieve sore muscles, stiff muscles and joints, head and back aches, cramps and athletic injuries. FDA UDI

Identifiers

Primary DI / UDI-DI
00708820523418 FDA UDI
FDA Product Code
IME FDA UDI
GMDN Term
Hot/cold therapy pack, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

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

Yes

FDA UDI

Dimensions & Sizes

Size
Area/Surface Area — 72 Square inch FDA UDI

Category: Hot/cold therapy pack, reusable

Meijer Hot & Cold Therapy Wrap with Clay Based Technology by Meijer, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI 6dda88db-a8dd-45bf-862a-fea4debf5f9d 36 fields · synced May 30, 2026