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Healthweigh

FDA UDI

Class I (US FDA UDI)

by Rice Lake Weighing Systems

Identity

Trade Name
Healthweigh FDA UDI
Generic Name
Patient-height measure FDA UDI
Device Name
Height Rod, 260-10-1 FDA UDI
Model / Reference
Height Rod FDA UDI
Description
Height Rod, 260-10-1 FDA UDI

Identifiers

Catalog Number
206553 FDA UDI
Primary DI / UDI-DI
00850042373392 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Patient-height measure FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient-height measure

Healthweigh by Rice Lake Weighing Systems — 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 c84592e4-7b52-4979-afac-c260e0202dc2 34 fields · synced May 30, 2026