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Detecto

FDA UDI

Class I (US FDA UDI)

by Cardinal Scale Manufacturing Company

Identity

Trade Name
Detecto FDA UDI
Generic Name
Patient-height measure FDA UDI
Device Name
icon Digital Clinical Scale, Wi-Fi, Sonar Height Rod, Includes Non-Medical-Grade AC Adapter FDA UDI
Model / Reference
ICON-WI FDA UDI
Description
icon Digital Clinical Scale, Wi-Fi, Sonar Height Rod, Includes Non-Medical-Grade AC Adapter FDA UDI

Identifiers

Primary DI / UDI-DI
00809161198904 FDA UDI
FDA Product Code
FRI FDA UDI
GMDN Term
Patient-height measure FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2700 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stand-on floor scale, electronicPatient-height measure

Detecto by Cardinal Scale Manufacturing Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient-height measure.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6260a516-eab3-4323-9c2e-b76dd4ab4024 33 fields · synced May 31, 2026