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Sharper Image

FDA UDI

Class II (US FDA UDI)

by Guangdong Okay Technology Co., Ltd.

Identity

Trade Name
SHARPER IMAGE FDA UDI
Generic Name
Electric pad localized-body heating system FDA UDI
Device Name
Calming Heat Back Wrap.Input DC 5V, 2A, Power 10W. Calming Heat Back Wrap(3settings). 3 Heat,9 Vibration,3 Lumbar. This device complies with part 15 of FCC rules. FDA UDI
Model / Reference
CHBWON-9 FDA UDI
Description
Calming Heat Back Wrap.Input DC 5V, 2A, Power 10W. Calming Heat Back Wrap(3settings). 3 Heat,9 Vibration,3 Lumbar. This device complies with part 15 of FCC rules. FDA UDI

Identifiers

Catalog Number
31801-31782 FDA UDI
Primary DI / UDI-DI
06936189900722 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Electric pad localized-body heating system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5740 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electric pad localized-body heating system

Sharper Image by Guangdong Okay Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric pad localized-body heating system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a782bdce-0271-4388-b1b7-40ed54421755 35 fields · synced May 30, 2026