← Back to catalogue

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
solo Digital Clinical Scale, Mechanical Height Rod, 550 lb x 0.2 lb / 250 kg x 0.1 kg FDA UDI
Model / Reference
Solo FDA UDI
Description
solo Digital Clinical Scale, Mechanical Height Rod, 550 lb x 0.2 lb / 250 kg x 0.1 kg FDA UDI

Identifiers

Primary DI / UDI-DI
00809161197709 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

Dimensions & Sizes

Size
Area/Surface Area — 210 Square inch 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c4b4d55f-71ee-4848-ac82-192555d9ca89 34 fields · synced May 31, 2026