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ColdSPOT

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 505

by Beekley Corporation

Identity

Trade Name
ColdSPOT EUDAMEDFDA UDI
Generic Name
Hot/cold therapy pack, single-use FDA UDI
Device Name
ColdSPOT EUDAMED
Cold Therapy Packs, 2.0x3.0" gel pack FDA UDI
Model / Reference
505 EUDAMEDFDA UDI
Description
Cold Therapy Packs, 2.0x3.0" gel pack FDA UDI

Identifiers

Primary DI / UDI-DI
00815137021060 EUDAMEDFDA UDI
Basic UDI-DI
00815137021060AZ EUDAMED
FDA Product Code
IMD FDA UDI
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED
GMDN Term
Hot/cold therapy pack, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.5710 FDA UDI
Medical Purpose
Cold Therapy Packs EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hot/cold therapy pack, reusable

ColdSPOT by Beekley Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beekley Corporation
EUDAMED SRN
US-PR-000044332

Sources (2)

  • EUDAMED e564b3f1-f136-4562-ba6d-6973481ee3e6 61 fields · synced Jun 8, 2026
  • FDA UDI 4de12c67-1fe1-41e5-9a44-cad8b4b15b22 33 fields · synced May 30, 2026