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Fukuda Denshi

FDA UDI

Class II (US FDA UDI)

by Fukuda Denshi Co., Ltd.

Identity

Trade Name
FUKUDA DENSHI FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Model / Reference
CMO-07FT-3NAB FDA UDI

Identifiers

Primary DI / UDI-DI
04538612911170 FDA UDI
510(k) Number
K150030 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

No

FDA UDI

Category: Electrocardiographic lead set, reusable

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

Similar devices

Also classified as Electrocardiographic lead set, reusable.

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 d2c826d1-de9b-4540-97f3-61fef86e11c2 33 fields · synced May 30, 2026