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Dickson Paraffin Bath

FDA UDI

Class II (US FDA UDI)

by Whitehall Manufacturing Co

Identity

Trade Name
Dickson Paraffin Bath FDA UDI
Generic Name
Physical therapy paraffin wax bath FDA UDI
Device Name
PB105-PARAFFIN BATH 220V INDIA/S.A. CORD FDA UDI
Model / Reference
PB-105B-CORD7 FDA UDI
Description
PB105-PARAFFIN BATH 220V INDIA/S.A. CORD FDA UDI

Identifiers

Catalog Number
PB105BCORD7 FDA UDI
Primary DI / UDI-DI
00645724004127 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

Dickson Paraffin Bath 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 980d2dc8-6537-427e-97db-098451b53da2 35 fields · synced Jun 1, 2026