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Floor Mat Sensors Tri-Fold

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Floor Mat Sensors Tri-Fold FDA UDI
Generic Name
Bed/chair occupant movement pressure/vibration sensor FDA UDI
Device Name
Dynarex Protech-24" x 48", Gray FDA UDI
Model / Reference
P-109950 FDA UDI
Description
Dynarex Protech-24" x 48", Gray FDA UDI

Identifiers

Primary DI / UDI-DI
00840117326200 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Bed/chair occupant movement pressure/vibration 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

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: Bed/chair occupant movement pressure/vibration sensor

Floor Mat Sensors Tri-Fold by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair occupant movement pressure/vibration sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 5845a118-73f0-45cb-90a5-6669e574460e 33 fields · synced Jun 6, 2026