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Reathlete

FDA UDI

Class II (US FDA UDI)

by Reathlete LLC

Identity

Trade Name
REATHLETE FDA UDI
Generic Name
Bed/chair electric massager FDA UDI
Model / Reference
FE-7204B FDA UDI

Identifiers

Primary DI / UDI-DI
00850020582464 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Bed/chair electric 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bed/chair electric massager

Reathlete by Reathlete LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair electric massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reathlete LLC

Sources (1)

  • FDA UDI 8aceed1d-e344-43fc-8c08-6863ea06a317 32 fields · synced Jun 7, 2026