← Back to catalogue

Coolject Topical Anesthetic Canister

FDA UDI

Class U (US FDA UDI)

by Vapocoolshot, Inc

Identity

Trade Name
Coolject Topical Anesthetic Canister FDA UDI
Generic Name
Cold/cool therapy spray FDA UDI
Device Name
Coolject Topical Anesthetic Canister FDA UDI
Model / Reference
VM02000-00 FDA UDI
Description
Coolject Topical Anesthetic Canister FDA UDI

Identifiers

Primary DI / UDI-DI
00860006961503 FDA UDI
510(k) Number
K193349 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cold/cool therapy spray

Coolject Topical Anesthetic Canister by Vapocoolshot, Inc — 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

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

Manufacturer
Vapocoolshot, Inc

Sources (1)

  • FDA UDI 5013d4a5-42d8-44b2-a8cf-0d9b0c4b021f 34 fields · synced May 31, 2026