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VCOMIN Fetal Doppler

FDA UDI

Class II (US FDA UDI)

by Vcomin Technlogy Limited

Identity

Trade Name
VCOMIN Fetal Doppler FDA UDI
Generic Name
Foetal Doppler system FDA UDI
Model / Reference
FD-231D FDA UDI

Identifiers

Primary DI / UDI-DI
00697044209003 FDA UDI
510(k) Number
K182526 FDA UDI
FDA Product Code
KNG FDA UDI
GMDN Term
Foetal Doppler system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2660 FDA UDI
Commercial Distribution
Not 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

VCOMIN Fetal Doppler by Vcomin Technlogy Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K182526 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vcomin Technlogy Limited

Sources (1)

  • FDA UDI e5513e5b-1291-4dd3-82bf-e18e9a58de8c 34 fields · synced Jun 8, 2026