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Whitehall Thermalators

FDA UDI

Class I (US FDA UDI)

by Whitehall Manufacturing Co

Identity

Trade Name
Whitehall Thermalators FDA UDI
Generic Name
Hot therapy pack heating unit FDA UDI
Device Name
T-4-S-EXE, TruMedical FDA UDI
Model / Reference
T-4-S-0010 FDA UDI
Description
T-4-S-EXE, TruMedical FDA UDI

Identifiers

Catalog Number
T-4-S-0020 FDA UDI
Primary DI / UDI-DI
00645724000686 FDA UDI
FDA Product Code
IRQ FDA UDI
GMDN Term
Hot therapy pack heating unit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5950 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Whitehall Thermalators by Whitehall Manufacturing Co — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b85cdcd6-4beb-4bda-96ac-677c770566f6 36 fields · synced Jun 1, 2026