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TheraFlo M-set 36'' × 80'' QLT Sentech

FDA UDI

Class II (US FDA UDI)

by Tridien Medical

Identity

Trade Name
TheraFlo M-set 36'' × 80'' QLT Sentech FDA UDI
Generic Name
Alternating-pressure bed mattress overlay, reusable FDA UDI
Device Name
TheraFlo M-set 36'' × 80'' QLT Sentech FDA UDI
Model / Reference
S2001-2200 FDA UDI
Description
TheraFlo M-set 36'' × 80'' QLT Sentech FDA UDI

Identifiers

Catalog Number
3001001 FDA UDI
Primary DI / UDI-DI
00841965103814 FDA UDI
FDA Product Code
IOQ FDA UDI
GMDN Term
Alternating-pressure bed mattress overlay, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5170 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Alternating-pressure bed mattress overlay, reusable

TheraFlo M-set 36'' × 80'' QLT Sentech by Tridien Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress overlay, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tridien Medical

Sources (1)

  • FDA UDI 456687f9-90e9-4e45-86fb-81e31271b91f 35 fields · synced May 30, 2026