Dynarex Protech String Fall Monitor

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Dynarex Protech String Fall Monitor FDA UDI
Generic Name: Ambulatory fall sensor FDA UDI
Device Name: Dynarex Protech String Fall Monitor FDA UDI
Model / Reference: P-800100 FDA UDI
Description: Dynarex Protech String Fall Monitor FDA UDI

Identifiers

Primary DI / UDI-DI: 00840117322936 FDA UDI
FDA Product Code: KMI FDA UDI
GMDN Term: Ambulatory fall sensor 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

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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Ambulatory fall sensor

Dynarex Protech String Fall Monitor by Dynarex Corp. — 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: Dynarex Corp.

Sources (1)

FDA UDI 06612f87-78ac-4d0a-84ef-f7da2ea08032 33 fields · synced May 31, 2026