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eMVFit

FDA UDI

Class II (US FDA UDI)

by Weero Co., Ltd.

Identity

Trade Name
eMVFit FDA UDI
Generic Name
Multi-modality physical therapy system, professional-use FDA UDI
Device Name
Pain management device with RF, Vacuum and EMS FDA UDI
Model / Reference
MVF-10M FDA UDI
Description
Pain management device with RF, Vacuum and EMS FDA UDI

Identifiers

Primary DI / UDI-DI
08809851470053 FDA UDI
510(k) Number
K240991 FDA UDI
K240992 FDA UDI
FDA Product Code
PBX FDA UDI
IPF FDA UDI
GMDN Term
Multi-modality physical therapy system, professional-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
890.5850 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

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
MRI Safety
MR Unsafe FDA UDI

Category: Multi-modality physical therapy system, professional-use

eMVFit by Weero Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality physical therapy system, professional-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Weero Co., Ltd.

Sources (1)

  • FDA UDI 964bed3c-f246-4f0c-bf28-ede80fd3a6fd 34 fields · synced Jun 8, 2026