CanarE – Clinic Wearable Device

FDA UDI

Class I (US FDA UDI)

by Canary Medical Usa Llc

Identity

Trade Name: CanarE – Clinic Wearable Device FDA UDI
Generic Name: Electronic goniometer/kinesiology sensor FDA UDI
Model / Reference: 43-5570-007-14 FDA UDI

Identifiers

Primary DI / UDI-DI: 00860003118344 FDA UDI
FDA Product Code: KQW FDA UDI
GMDN Term: Electronic goniometer/kinesiology sensor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1520 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Electronic goniometer/kinesiology sensor

CanarE – Clinic Wearable Device by Canary Medical Usa Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Canary Medical Usa Llc

Sources (1)

FDA UDI 3c0becbf-8331-4029-b023-3aed0b17a52f 32 fields · synced May 30, 2026