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Motionciser

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 09Model MC-001

by Guangzhou Xinbo Electronic Co., Ltd

Identity

Trade Name
Motionciser EUDAMED
DR-HOS FDA UDI
Generic Name
Vibration platform exerciser, stationary FDA UDI
Device Name
Motionciser EUDAMED
XJ-F-30 FDA UDI
Model / Reference
MC-001 EUDAMED
09 EUDAMED
Motionciser FDA UDI
Description
XJ-F-30 FDA UDI

Identifiers

Primary DI / UDI-DI
06970742220339 EUDAMEDFDA UDI
Basic UDI-DI
697074222MCYR EUDAMED
FDA Product Code
ISA FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Vibration platform exerciser, stationary FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.5660 FDA UDI
Market of Registration
Netherlands EUDAMED
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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Device sterilization/disinfection container, reusable

Motionciser by Guangzhou Xinbo Electronic Co., Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000012183
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (2)

  • EUDAMED b96c9f17-490d-4397-b189-857843971d68 61 fields · synced Jun 18, 2026
  • FDA UDI aa9b9361-3a07-48db-9964-9425bd2ba5ee 33 fields · synced May 30, 2026