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stratosphere

FDA UDI

Class I (US FDA UDI)

by Saxony Beauty Technology GmbH

Identity

Trade Name
stratosphere FDA UDI
Generic Name
Hand-held electric massager FDA UDI
Device Name
Massager for body sculpting and anti-cellulite procedures. FDA UDI
Model / Reference
Smart FDA UDI
Description
Massager for body sculpting and anti-cellulite procedures. FDA UDI

Identifiers

Catalog Number
TMSTRSM04 FDA UDI
Primary DI / UDI-DI
04262384030035 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Hand-held 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 50 Centimeter FDA UDI
Width — 41 Centimeter FDA UDI
Height — 101 Centimeter FDA UDI

Category: Hand-held electric massager

stratosphere by Saxony Beauty Technology GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held electric massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cfa27591-0520-41bf-8405-31a41b1326c0 37 fields · synced May 30, 2026