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Medi-First Cold Spray

FDA UDI

Class U (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Cold Spray FDA UDI
Generic Name
Cold/cool therapy spray FDA UDI
Device Name
A non-sterile liquid in a spray container intended for localized application to the body surface to provide a cooling effect. FDA UDI
Model / Reference
23017 FDA UDI
Description
A non-sterile liquid in a spray container intended for localized application to the body surface to provide a cooling effect. FDA UDI

Identifiers

Catalog Number
23017 FDA UDI
Primary DI / UDI-DI
00347682230173 FDA UDI
510(k) Number
K033720 FDA UDI
FDA Product Code
MLY FDA UDI
GMDN Term
Cold/cool therapy spray FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cold/cool therapy spray

Medi-First Cold Spray by Medique Products — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cold/cool therapy spray.

Cleared under the same submission

K033720 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI d947fc2e-8659-4ecc-bba2-f552a2efb1fc 36 fields · synced May 30, 2026