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Convex probe

FDA UDI

Class II (US FDA UDI)

by CHISON Medical Technologies Co., Ltd.

Identity

Trade Name
Convex probe FDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Model / Reference
M3C60L FDA UDI

Identifiers

Primary DI / UDI-DI
06945121400138 FDA UDI
510(k) Number
K153085 FDA UDI
FDA Product Code
ITX 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
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

Category: Extracorporeal ultrasound imaging transducer, hand-held

Convex probe by CHISON Medical Technologies 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.

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 12c8f1ec-92d4-4a26-a691-d8bc7e2abde1 33 fields · synced Jun 8, 2026