Detecto

FDA UDI

Class I (US FDA UDI)

by Cardinal Scale Manufacturing Company

Identity

Trade Name: Detecto FDA UDI
Generic Name: Bed scale FDA UDI
Device Name: Stretcher Scale, Portable, Digital, 800 lb x .2 lb / 360 kg x .1 kg FDA UDI
Model / Reference: 8500 FDA UDI
Description: Stretcher Scale, Portable, Digital, 800 lb x .2 lb / 360 kg x .1 kg FDA UDI

Identifiers

Primary DI / UDI-DI: 00809161305005 FDA UDI
FDA Product Code: FRW FDA UDI
GMDN Term: Bed scale FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.2720 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: Bed 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 8757a78e-755f-4f5b-9ce3-4bbe81a8169f 33 fields · synced Jun 1, 2026