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medisana

FDA UDI

Class II (US FDA UDI)

by Zhangzhou Easepal Innovation Co., Ltd.

Identity

Trade Name
medisana FDA UDI
Generic Name
Pneumatic massager FDA UDI
Device Name
Leg Massager FDA UDI
Model / Reference
EP-1129 FDA UDI
Description
Leg Massager FDA UDI

Identifiers

Primary DI / UDI-DI
06973534130229 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Pneumatic massager FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pneumatic massager

medisana by Zhangzhou Easepal Innovation Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhangzhou Easepal Innovation Co., Ltd.

Sources (1)

  • FDA UDI b8e074e4-4795-4ca5-b732-0f41c0432925 33 fields · synced May 29, 2026