← Back to catalogue

Cramer Instant Cold Pack

FDA UDI

Class I (US FDA UDI)

by Cramer Products, Inc.

Identity

Trade Name
Cramer Instant Cold Pack FDA UDI
Generic Name
Endothermic cold therapy pack FDA UDI
Device Name
Pack, Hot or Cold, Disposable FDA UDI
Model / Reference
033101 FDA UDI
Description
Pack, Hot or Cold, Disposable FDA UDI

Identifiers

Primary DI / UDI-DI
00311960410304 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 9 Inch FDA UDI
Width — 6 Inch FDA UDI

Category: Endothermic cold therapy pack

Cramer Instant Cold Pack by Cramer Products, Inc. — 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

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

Manufacturer

Sources (1)

  • FDA UDI 8fd5ac1e-33c8-4907-8639-e7577f795773 35 fields · synced Jun 1, 2026