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No

FDA UDI

Class I (US FDA UDI)

by Shenzhen As-Tec Technology Co., Ltd.

Identity

Trade Name
NO FDA UDI
Generic Name
Freestanding electric massager FDA UDI
Device Name
the foot massager with vibration and heat is provide temporary relief from stress, fatique and soreness in the feet. As an added feature, you may use the included electrode cables, belt to administer massage to other parts of the body, including the legs, arms, back, etc. FDA UDI
Model / Reference
AS816 FDA UDI
Description
the foot massager with vibration and heat is provide temporary relief from stress, fatique and soreness in the feet. As an added feature, you may use the included electrode cables, belt to administer massage to other parts of the body, including the legs, arms, back, etc. FDA UDI

Identifiers

Primary DI / UDI-DI
06970890320622 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Freestanding electric massager FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Freestanding electric massager

No by Shenzhen As-Tec Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding electric massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d099048f-3aa1-4c06-991f-a53cf943a9a5 35 fields · synced May 30, 2026