← Back to catalogue

Whitehall Thermalators

FDA UDI

Class I (US FDA UDI)

by Whitehall Manufacturing Co

Identity

Trade Name
Whitehall Thermalators FDA UDI
Generic Name
Cold therapy pack chilling unit FDA UDI
Device Name
CRYO DERMA, 6 PACK, STATIONARY 220V FDA UDI
Model / Reference
T-6-S-220V_CRYO FDA UDI
Description
CRYO DERMA, 6 PACK, STATIONARY 220V FDA UDI

Identifiers

Catalog Number
T6S220VCRYO FDA UDI
Primary DI / UDI-DI
00645724003878 FDA UDI
FDA Product Code
IRQ FDA UDI
GMDN Term
Cold therapy pack chilling unit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5950 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: Hot therapy pack heating unitCold therapy pack chilling unit

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

Similar devices

Also classified as Cold therapy pack chilling unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9d3a0b7f-c5eb-4a57-8054-c3087894be15 35 fields · synced Jun 1, 2026