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Rego Safe Mobility App

FDA UDI

Class I (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
Rego Safe Mobility App FDA UDI
Generic Name
Inpatient motion surveillance software FDA UDI
Model / Reference
Rego Safe Mobility App FDA UDI

Identifiers

Primary DI / UDI-DI
00840828192095 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Inpatient motion surveillance software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 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

Yes

FDA UDI

Category: Inpatient motion surveillance software

Rego Safe Mobility App by Curbell Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inpatient motion surveillance software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1df284b9-d3e2-4238-942e-4fe9deb7662e 33 fields · synced May 30, 2026