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Green GuardInstant Cold Pack

FDA UDI

Class I (US FDA UDI)

by Greenguard

Identity

Trade Name
Green GuardInstant Cold Pack FDA UDI
Generic Name
Endothermic cold therapy pack FDA UDI
Device Name
A device intended to be applied with pressure to the body surface to provide cold therapy - Medium FDA UDI
Model / Reference
3302 FDA UDI
Description
A device intended to be applied with pressure to the body surface to provide cold therapy - Medium FDA UDI

Identifiers

Catalog Number
3302 FDA UDI
Primary DI / UDI-DI
00347682033026 FDA UDI
FDA Product Code
IMD FDA UDI
GMDN Term
Endothermic cold therapy pack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5710 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA 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: Endothermic cold therapy pack

Green GuardInstant Cold Pack by Greenguard — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endothermic cold therapy pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Greenguard

Sources (1)

  • FDA UDI 2876a2e3-c745-4c11-aa86-1fb55ea352dd 36 fields · synced Jun 1, 2026