Identity
- Trade Name
- D-ACTOR 100 EUDAMEDD-ACTOR® FDA UDI
- Generic Name
- Hand-held electric massager FDA UDI
- Device Name
- D-ACTOR 100 EUDAMEDPulse Activation Therapy System FDA UDI
- Model / Reference
- 23300.0103 EUDAMED100 FDA UDI
- Description
- Pulse Activation Therapy System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07630039101060 EUDAMEDFDA UDI
- Basic UDI-DI
- B-07630039101060 EUDAMED
- 510(k) Number
- K173692 FDA UDI
- FDA Product Code
- ISA FDA UDI
- EMDN Code
- Z120622,Z12139001 EUDAMED
- GMDN Term
- Hand-held electric massager FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 890.5660 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Hand-held electric massagerPressure-wave skin/body contouring system
D-Actor® by Storz Medical AG — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Pressure-wave skin/body contouring system.
- Slimspec — Medispec, Ltd. · Class I
- D-ACTOR® — Storz Medical AG · Class I
- MASTERPULS® — Storz Medical AG · Class I
- D-ACTOR® — Storz Medical AG · Class I
- DUOLITH® — Storz Medical AG · Class I
Cleared under the same submission
K173692 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Storz Medical AG
Sources (2)
- FDA UDI 88000f1f-e7ac-4d6a-9a80-a20430de443e 34 fields · synced Jun 11, 2026
- EUDAMED fc150be1-7060-4427-9220-2c966b7b755f 61 fields · synced Jun 11, 2026