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veicomtech

FDA UDI

Class II (US FDA UDI)

by Guangzhou Huakai Electronic Technology Co., Ltd.

Identity

Trade Name
veicomtech FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
Ems Foot Stimulator FDA UDI
Model / Reference
HK701 FDA UDI
Description
Ems Foot Stimulator FDA UDI

Identifiers

Primary DI / UDI-DI
06974241370366 FDA UDI
510(k) Number
K221251 FDA UDI
FDA Product Code
NUH FDA UDI
IRT FDA UDI
NGX FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
890.5740 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Physical therapy transcutaneous neuromuscular electrical stimulation system

veicomtech by Guangzhou Huakai Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy transcutaneous neuromuscular electrical stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a59d289-e90f-48eb-93f5-198fcca11db2 34 fields · synced Jun 8, 2026