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Thermasplint

FDA UDI

Class II (US FDA UDI)

by Whitehall Manufacturing Co

Identity

Trade Name
Thermasplint FDA UDI
Generic Name
Physical therapy paraffin wax bath FDA UDI
Device Name
FORMA SPLINT WITH 220V POWER CORD(LG) FDA UDI
Model / Reference
SP-1502B_AMBER FDA UDI
Description
FORMA SPLINT WITH 220V POWER CORD(LG) FDA UDI

Identifiers

Catalog Number
SP1502BAMBER FDA UDI
Primary DI / UDI-DI
00645724004226 FDA UDI
FDA Product Code
IMC FDA UDI
GMDN Term
Physical therapy paraffin wax bath FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5110 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Physical therapy paraffin wax bath

Thermasplint by Whitehall Manufacturing Co — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy paraffin wax bath.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af662ea4-4067-4f1d-b12a-863f35df7413 35 fields · synced May 30, 2026