Detecto

FDA UDI

Class I (US FDA UDI)

by Cardinal Scale Manufacturing Company

Identity

Trade Name: Detecto FDA UDI
Generic Name: Wheelchair-accessible platform scale FDA UDI
Device Name: Scale, Wheelchair, Folding, w/ AC Adapter, OIML EC Class III 300 kg x 0.1 kg, FDA UDI
Model / Reference: 6550KGEU-AC FDA UDI
Description: Scale, Wheelchair, Folding, w/ AC Adapter, OIML EC Class III 300 kg x 0.1 kg, FDA UDI

Identifiers

Primary DI / UDI-DI: 00809161307405 FDA UDI
FDA Product Code: INF FDA UDI
GMDN Term: Wheelchair-accessible platform scale FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3940 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

Category: Wheelchair-accessible platform scale

Detecto by Cardinal Scale Manufacturing Company — 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: Cardinal Scale Manufacturing Company

Sources (1)

FDA UDI 2281837c-acbb-43fe-b4b7-ae4de7c1d44a 33 fields · synced Jun 1, 2026