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Med One

FDA UDI

Class I (US FDA UDI)

by Shenzhen Urion Technology Co., Ltd.

Identity

Trade Name
Med One FDA UDI
Generic Name
Wearable electric massager FDA UDI
Model / Reference
UM605 FDA UDI

Identifiers

Catalog Number
Yes FDA UDI
Primary DI / UDI-DI
06953825908751 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Wearable 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

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

Category: Wearable electric massager

Med One by Shenzhen Urion Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable electric massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shenzhen Urion Technology Co., Ltd.

Sources (1)

  • FDA UDI 77428656-2c0a-452c-bfe6-60b98161afea 33 fields · synced Jun 8, 2026