Identity
- Trade Name
- SHARPER IMAGE FDA UDI
- Generic Name
- Hand-held electric massager FDA UDI
- Device Name
- Calming heat Deluxe massaging Flexi Wrap. Input DC 5V, 1A, Power 5W. Heat 3 gears ,Shake 9 gears . This device complies with part 15 of FCC rules. FDA UDI
- Model / Reference
- 25in CHFWU-9 FDA UDI
- Description
- Calming heat Deluxe massaging Flexi Wrap. Input DC 5V, 1A, Power 5W. Heat 3 gears ,Shake 9 gears . This device complies with part 15 of FCC rules. FDA UDI
Identifiers
- Catalog Number
- CWT24003 FDA UDI
- Primary DI / UDI-DI
- 06936189900685 FDA UDI
- FDA Product Code
- IRT FDA UDI
- GMDN Term
- Hand-held electric massager 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Hand-held electric massager
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 Hand-held electric massager.
- Massage Gun — ShenZhen Pentasmart Technology Co, .Ltd · Class I
- G5® — GENERAL PHYSIOTHERAPY INC · Class I
- D-ACTOR® — Storz Medical AG · Class I
- RENPHO Eye Massager — JOICOM CORPORATION · Class I
- Maptag — Sanwei Taige (Suzhou) Medical Co., Ltd. · Class I
- Homedics — Health Care Massage Branch of Zhangzhou Easepal Industrial Co., Ltd. · Class I
- PM-750 — PRO MEDICAL SUPPLIES, INC. · Class I
- Homedics — ZHANGZHOU EASEPAL INNOVATION CO., LTD. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Guangdong Okay Technology Co., Ltd.
Sources (1)
- FDA UDI a5bb350b-a64a-4412-9709-b6679bd79c31 35 fields · synced May 30, 2026