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Mp1-5x

FDA UDI

Class II (US FDA UDI)

by Alpinion Medical Systems Co., Ltd.

Identity

Trade Name
MP1-5X FDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Model / Reference
MP1-5X FDA UDI

Identifiers

Primary DI / UDI-DI
08800013512055 FDA UDI
FDA Product Code
ITX FDA UDI
IYO FDA UDI
IYN FDA UDI
GMDN Term
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.1560 FDA UDI
892.1550 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Extracorporeal ultrasound imaging transducer, hand-held

Mp1-5x by Alpinion Medical Systems Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extracorporeal ultrasound imaging transducer, hand-held.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ec9fdbf3-c22e-4a50-805b-828f4e5dde6a 32 fields · synced May 30, 2026