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ProFit

FDA UDI

Class I (US FDA UDI)

by Therafin Corporation

Identity

Trade Name
ProFit FDA UDI
Generic Name
Wheelchair/chair/stander headrest FDA UDI
Device Name
HEADREST PAD, PRO-FIT 5X14" SOFT WITH SMOOTH COVER, LARGE. FDA UDI
Model / Reference
50367 FDA UDI
Description
HEADREST PAD, PRO-FIT 5X14" SOFT WITH SMOOTH COVER, LARGE. FDA UDI

Identifiers

Catalog Number
50367 FDA UDI
Primary DI / UDI-DI
00840252901256 FDA UDI
FDA Product Code
IMS FDA UDI
GMDN Term
Wheelchair/chair/stander headrest FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3910 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: Wheelchair/chair/stander headrest

ProFit by Therafin Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair/chair/stander headrest.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bfa81b52-c3d1-4354-a6bf-c40ddbaa7ba7 35 fields · synced Jun 8, 2026